Canonical Allele Identifier: CA2659545389
Gene: DYSF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71526416_71526417insGGGGGGGGGGGGGGGGGGGGGGT , CM000664.2:g.71526416_71526417insGGGGGGGGGGGGGGGGGGGGGGT GRCh38
NC_000002.11:g.71753546_71753547insGGGGGGGGGGGGGGGGGGGGGGT , CM000664.1:g.71753546_71753547insGGGGGGGGGGGGGGGGGGGGGGT GRCh37
NC_000002.10:g.71607054_71607055insGGGGGGGGGGGGGGGGGGGGGGT NCBI36
NG_008694.1:g.77794_77795insGGGGGGGGGGGGGGGGGGGGGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000258104.8:c.1180+70_1180+71insGGGGGGGGGGGGGGGGGGGGGGT MANE Plus Clinical ENSP00000258104.3:n.1180+70_1180+71insGGGGGGGGGGGGGGGGGGGGGGT...
ENST00000410020.8:c.1276+70_1276+71insGGGGGGGGGGGGGGGGGGGGGGT MANE Select ENSP00000386881.3:n.1276+70_1276+71insGGGGGGGGGGGGGGGGGGGGGGT...
ENST00000258104.7:c.1180+70_1180+71insGGGGGGGGGGGGGGGGGGGGGGT ENSP00000258104.3:n.1180+70_1180+71insGGGGGGGGGGGGGGGGGGGGGGT...
ENST00000394120.6:c.1183+70_1183+71insGGGGGGGGGGGGGGGGGGGGGGT ENSP00000377678.2:n.1183+70_1183+71insGGGGGGGGGGGGGGGGGGGGGGT...
ENST00000409366.5:c.1183+70_1183+71insGGGGGGGGGGGGGGGGGGGGGGT ENSP00000386512.1:n.1183+70_1183+71insGGGGGGGGGGGGGGGGGGGGGGT...
ENST00000409582.7:c.1273+70_1273+71insGGGGGGGGGGGGGGGGGGGGGGT ENSP00000386547.3:n.1273+70_1273+71insGGGGGGGGGGGGGGGGGGGGGGT...
ENST00000409651.5:c.1276+70_1276+71insGGGGGGGGGGGGGGGGGGGGGGT ENSP00000386683.1:n.1276+70_1276+71insGGGGGGGGGGGGGGGGGGGGGGT...
ENST00000409744.5:c.1183+70_1183+71insGGGGGGGGGGGGGGGGGGGGGGT ENSP00000386285.1:n.1183+70_1183+71insGGGGGGGGGGGGGGGGGGGGGGT...
ENST00000409762.5:c.1273+70_1273+71insGGGGGGGGGGGGGGGGGGGGGGT ENSP00000387137.1:n.1273+70_1273+71insGGGGGGGGGGGGGGGGGGGGGGT...
ENST00000410020.7:c.1276+70_1276+71insGGGGGGGGGGGGGGGGGGGGGGT ENSP00000386881.3:n.1276+70_1276+71insGGGGGGGGGGGGGGGGGGGGGGT...
ENST00000410041.1:c.1276+70_1276+71insGGGGGGGGGGGGGGGGGGGGGGT ENSP00000386617.1:n.1276+70_1276+71insGGGGGGGGGGGGGGGGGGGGGGT...
ENST00000413539.6:c.1273+70_1273+71insGGGGGGGGGGGGGGGGGGGGGGT ENSP00000407046.2:n.1273+70_1273+71insGGGGGGGGGGGGGGGGGGGGGGT...
ENST00000429174.6:c.1180+70_1180+71insGGGGGGGGGGGGGGGGGGGGGGT ENSP00000398305.2:n.1180+70_1180+71insGGGGGGGGGGGGGGGGGGGGGGT...
NM_001130455.1:c.1183+70_1183+71insGGGGGGGGGGGGGGGGGGGGGGT NP_001123927.1:n.1183+70_1183+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_001130976.1:c.1180+70_1180+71insGGGGGGGGGGGGGGGGGGGGGGT NP_001124448.1:n.1180+70_1180+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_001130977.1:c.1180+70_1180+71insGGGGGGGGGGGGGGGGGGGGGGT NP_001124449.1:n.1180+70_1180+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_001130978.1:c.1180+70_1180+71insGGGGGGGGGGGGGGGGGGGGGGT NP_001124450.1:n.1180+70_1180+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_001130979.1:c.1273+70_1273+71insGGGGGGGGGGGGGGGGGGGGGGT NP_001124451.1:n.1273+70_1273+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_001130980.1:c.1273+70_1273+71insGGGGGGGGGGGGGGGGGGGGGGT NP_001124452.1:n.1273+70_1273+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_001130981.1:c.1273+70_1273+71insGGGGGGGGGGGGGGGGGGGGGGT NP_001124453.1:n.1273+70_1273+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_001130982.1:c.1276+70_1276+71insGGGGGGGGGGGGGGGGGGGGGGT NP_001124454.1:n.1276+70_1276+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_001130983.1:c.1183+70_1183+71insGGGGGGGGGGGGGGGGGGGGGGT NP_001124455.1:n.1183+70_1183+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_001130984.1:c.1183+70_1183+71insGGGGGGGGGGGGGGGGGGGGGGT NP_001124456.1:n.1183+70_1183+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_001130985.1:c.1276+70_1276+71insGGGGGGGGGGGGGGGGGGGGGGT NP_001124457.1:n.1276+70_1276+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_001130986.1:c.1183+70_1183+71insGGGGGGGGGGGGGGGGGGGGGGT NP_001124458.1:n.1183+70_1183+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_001130987.1:c.1276+70_1276+71insGGGGGGGGGGGGGGGGGGGGGGT NP_001124459.1:n.1276+70_1276+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_003494.3:c.1180+70_1180+71insGGGGGGGGGGGGGGGGGGGGGGT NP_003485.1:n.1180+70_1180+71insGGGGGGGGGGGGGGGGGGGGGGT
XM_005264584.3:c.1276+70_1276+71insGGGGGGGGGGGGGGGGGGGGGGT XP_005264641.1:n.1276+70_1276+71insGGGGGGGGGGGGGGGGGGGGGGT
XM_005264585.3:c.1273+70_1273+71insGGGGGGGGGGGGGGGGGGGGGGT XP_005264642.1:n.1273+70_1273+71insGGGGGGGGGGGGGGGGGGGGGGT
XM_005264584.4:c.1276+70_1276+71insGGGGGGGGGGGGGGGGGGGGGGT XP_005264641.1:n.1276+70_1276+71insGGGGGGGGGGGGGGGGGGGGGGT
XM_005264585.5:c.1273+70_1273+71insGGGGGGGGGGGGGGGGGGGGGGT XP_005264642.1:n.1273+70_1273+71insGGGGGGGGGGGGGGGGGGGGGGT
XR_001738969.1:n.1434+70_1434+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_001130987.2:c.1276+70_1276+71insGGGGGGGGGGGGGGGGGGGGGGT MANE Select NP_001124459.1:n.1276+70_1276+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_001130455.2:c.1183+70_1183+71insGGGGGGGGGGGGGGGGGGGGGGT NP_001123927.1:n.1183+70_1183+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_001130976.2:c.1180+70_1180+71insGGGGGGGGGGGGGGGGGGGGGGT NP_001124448.1:n.1180+70_1180+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_001130977.2:c.1180+70_1180+71insGGGGGGGGGGGGGGGGGGGGGGT NP_001124449.1:n.1180+70_1180+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_001130978.2:c.1180+70_1180+71insGGGGGGGGGGGGGGGGGGGGGGT NP_001124450.1:n.1180+70_1180+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_001130979.2:c.1273+70_1273+71insGGGGGGGGGGGGGGGGGGGGGGT NP_001124451.1:n.1273+70_1273+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_001130980.2:c.1273+70_1273+71insGGGGGGGGGGGGGGGGGGGGGGT NP_001124452.1:n.1273+70_1273+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_001130981.2:c.1273+70_1273+71insGGGGGGGGGGGGGGGGGGGGGGT NP_001124453.1:n.1273+70_1273+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_001130982.2:c.1276+70_1276+71insGGGGGGGGGGGGGGGGGGGGGGT NP_001124454.1:n.1276+70_1276+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_001130983.2:c.1183+70_1183+71insGGGGGGGGGGGGGGGGGGGGGGT NP_001124455.1:n.1183+70_1183+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_001130984.2:c.1183+70_1183+71insGGGGGGGGGGGGGGGGGGGGGGT NP_001124456.1:n.1183+70_1183+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_001130985.2:c.1276+70_1276+71insGGGGGGGGGGGGGGGGGGGGGGT NP_001124457.1:n.1276+70_1276+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_001130986.2:c.1183+70_1183+71insGGGGGGGGGGGGGGGGGGGGGGT NP_001124458.1:n.1183+70_1183+71insGGGGGGGGGGGGGGGGGGGGGGT
NM_003494.4:c.1180+70_1180+71insGGGGGGGGGGGGGGGGGGGGGGT MANE Plus Clinical NP_003485.1:n.1180+70_1180+71insGGGGGGGGGGGGGGGGGGGGGGT