Canonical Allele Identifier: CA275391
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 198458
dbSNP Id: rs794727851

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71515749G>T , CM000664.2:g.71515749G>T GRCh38
NC_000002.11:g.71742879G>T , CM000664.1:g.71742879G>T GRCh37
NC_000002.10:g.71596387G>T NCBI36
NG_008694.1:g.67127G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000258104.8:c.790G>T MANE Plus Clinical ENSP00000258104.3:p.Glu264Ter
ENST00000410020.8:c.886G>T MANE Select ENSP00000386881.3:p.Glu296Ter
ENST00000258104.7:c.790G>T ENSP00000258104.3:p.Glu264Ter
ENST00000394120.6:c.793G>T ENSP00000377678.2:p.Glu265Ter
ENST00000409366.5:c.793G>T ENSP00000386512.1:p.Glu265Ter
ENST00000409582.7:c.883G>T ENSP00000386547.3:p.Glu295Ter
ENST00000409651.5:c.886G>T ENSP00000386683.1:p.Glu296Ter
ENST00000409744.5:c.793G>T ENSP00000386285.1:p.Glu265Ter
ENST00000409762.5:c.883G>T ENSP00000387137.1:p.Glu295Ter
ENST00000410020.7:c.886G>T ENSP00000386881.3:p.Glu296Ter
ENST00000410041.1:c.886G>T ENSP00000386617.1:p.Glu296Ter
ENST00000413539.6:c.883G>T ENSP00000407046.2:p.Glu295Ter
ENST00000429174.6:c.790G>T ENSP00000398305.2:p.Glu264Ter
NM_001130455.1:c.793G>T NP_001123927.1:p.Glu265Ter
NM_001130976.1:c.790G>T NP_001124448.1:p.Glu264Ter
NM_001130977.1:c.790G>T NP_001124449.1:p.Glu264Ter
NM_001130978.1:c.790G>T NP_001124450.1:p.Glu264Ter
NM_001130979.1:c.883G>T NP_001124451.1:p.Glu295Ter
NM_001130980.1:c.883G>T NP_001124452.1:p.Glu295Ter
NM_001130981.1:c.883G>T NP_001124453.1:p.Glu295Ter
NM_001130982.1:c.886G>T NP_001124454.1:p.Glu296Ter
NM_001130983.1:c.793G>T NP_001124455.1:p.Glu265Ter
NM_001130984.1:c.793G>T NP_001124456.1:p.Glu265Ter
NM_001130985.1:c.886G>T NP_001124457.1:p.Glu296Ter
NM_001130986.1:c.793G>T NP_001124458.1:p.Glu265Ter
NM_001130987.1:c.886G>T NP_001124459.1:p.Glu296Ter
NM_003494.3:c.790G>T NP_003485.1:p.Glu264Ter
XM_005264584.3:c.886G>T XP_005264641.1:p.Glu296Ter
XM_005264585.3:c.883G>T XP_005264642.1:p.Glu295Ter
XM_005264584.4:c.886G>T XP_005264641.1:p.Glu296Ter
XM_005264585.5:c.883G>T XP_005264642.1:p.Glu295Ter
XR_001738969.1:n.1044G>T
NM_001130987.2:c.886G>T MANE Select NP_001124459.1:p.Glu296Ter
NM_001130455.2:c.793G>T NP_001123927.1:p.Glu265Ter
NM_001130976.2:c.790G>T NP_001124448.1:p.Glu264Ter
NM_001130977.2:c.790G>T NP_001124449.1:p.Glu264Ter
NM_001130978.2:c.790G>T NP_001124450.1:p.Glu264Ter
NM_001130979.2:c.883G>T NP_001124451.1:p.Glu295Ter
NM_001130980.2:c.883G>T NP_001124452.1:p.Glu295Ter
NM_001130981.2:c.883G>T NP_001124453.1:p.Glu295Ter
NM_001130982.2:c.886G>T NP_001124454.1:p.Glu296Ter
NM_001130983.2:c.793G>T NP_001124455.1:p.Glu265Ter
NM_001130984.2:c.793G>T NP_001124456.1:p.Glu265Ter
NM_001130985.2:c.886G>T NP_001124457.1:p.Glu296Ter
NM_001130986.2:c.793G>T NP_001124458.1:p.Glu265Ter
NM_003494.4:c.790G>T MANE Plus Clinical NP_003485.1:p.Glu264Ter