Canonical Allele Identifier: CA2659545002

Gene: DYSF

Linked Data

• gnomAD v4: 2-71526375-GTCTGCAGGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71526376_71526384del , CM000664.2:g.71526376_71526384del	GRCh38
NC_000002.11:g.71753506_71753514del , CM000664.1:g.71753506_71753514del	GRCh37
NC_000002.10:g.71607014_71607022del	NCBI36
NG_008694.1:g.77754_77762del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258104.8:c.1180+30_1180+38del MANE Plus Clinical	ENSP00000258104.3:n.1180+30_1180+38del
ENST00000410020.8:c.1276+30_1276+38del MANE Select	ENSP00000386881.3:n.1276+30_1276+38del
ENST00000258104.7:c.1180+30_1180+38del	ENSP00000258104.3:n.1180+30_1180+38del
ENST00000394120.6:c.1183+30_1183+38del	ENSP00000377678.2:n.1183+30_1183+38del
ENST00000409366.5:c.1183+30_1183+38del	ENSP00000386512.1:n.1183+30_1183+38del
ENST00000409582.7:c.1273+30_1273+38del	ENSP00000386547.3:n.1273+30_1273+38del
ENST00000409651.5:c.1276+30_1276+38del	ENSP00000386683.1:n.1276+30_1276+38del
ENST00000409744.5:c.1183+30_1183+38del	ENSP00000386285.1:n.1183+30_1183+38del
ENST00000409762.5:c.1273+30_1273+38del	ENSP00000387137.1:n.1273+30_1273+38del
ENST00000410020.7:c.1276+30_1276+38del	ENSP00000386881.3:n.1276+30_1276+38del
ENST00000410041.1:c.1276+30_1276+38del	ENSP00000386617.1:n.1276+30_1276+38del
ENST00000413539.6:c.1273+30_1273+38del	ENSP00000407046.2:n.1273+30_1273+38del
ENST00000429174.6:c.1180+30_1180+38del	ENSP00000398305.2:n.1180+30_1180+38del
NM_001130455.1:c.1183+30_1183+38del	NP_001123927.1:n.1183+30_1183+38del
NM_001130976.1:c.1180+30_1180+38del	NP_001124448.1:n.1180+30_1180+38del
NM_001130977.1:c.1180+30_1180+38del	NP_001124449.1:n.1180+30_1180+38del
NM_001130978.1:c.1180+30_1180+38del	NP_001124450.1:n.1180+30_1180+38del
NM_001130979.1:c.1273+30_1273+38del	NP_001124451.1:n.1273+30_1273+38del
NM_001130980.1:c.1273+30_1273+38del	NP_001124452.1:n.1273+30_1273+38del
NM_001130981.1:c.1273+30_1273+38del	NP_001124453.1:n.1273+30_1273+38del
NM_001130982.1:c.1276+30_1276+38del	NP_001124454.1:n.1276+30_1276+38del
NM_001130983.1:c.1183+30_1183+38del	NP_001124455.1:n.1183+30_1183+38del
NM_001130984.1:c.1183+30_1183+38del	NP_001124456.1:n.1183+30_1183+38del
NM_001130985.1:c.1276+30_1276+38del	NP_001124457.1:n.1276+30_1276+38del
NM_001130986.1:c.1183+30_1183+38del	NP_001124458.1:n.1183+30_1183+38del
NM_001130987.1:c.1276+30_1276+38del	NP_001124459.1:n.1276+30_1276+38del
NM_003494.3:c.1180+30_1180+38del	NP_003485.1:n.1180+30_1180+38del
XM_005264584.3:c.1276+30_1276+38del	XP_005264641.1:n.1276+30_1276+38del
XM_005264585.3:c.1273+30_1273+38del	XP_005264642.1:n.1273+30_1273+38del
XM_005264584.4:c.1276+30_1276+38del	XP_005264641.1:n.1276+30_1276+38del
XM_005264585.5:c.1273+30_1273+38del	XP_005264642.1:n.1273+30_1273+38del
XR_001738969.1:n.1434+30_1434+38del
NM_001130987.2:c.1276+30_1276+38del MANE Select	NP_001124459.1:n.1276+30_1276+38del
NM_001130455.2:c.1183+30_1183+38del	NP_001123927.1:n.1183+30_1183+38del
NM_001130976.2:c.1180+30_1180+38del	NP_001124448.1:n.1180+30_1180+38del
NM_001130977.2:c.1180+30_1180+38del	NP_001124449.1:n.1180+30_1180+38del
NM_001130978.2:c.1180+30_1180+38del	NP_001124450.1:n.1180+30_1180+38del
NM_001130979.2:c.1273+30_1273+38del	NP_001124451.1:n.1273+30_1273+38del
NM_001130980.2:c.1273+30_1273+38del	NP_001124452.1:n.1273+30_1273+38del
NM_001130981.2:c.1273+30_1273+38del	NP_001124453.1:n.1273+30_1273+38del
NM_001130982.2:c.1276+30_1276+38del	NP_001124454.1:n.1276+30_1276+38del
NM_001130983.2:c.1183+30_1183+38del	NP_001124455.1:n.1183+30_1183+38del
NM_001130984.2:c.1183+30_1183+38del	NP_001124456.1:n.1183+30_1183+38del
NM_001130985.2:c.1276+30_1276+38del	NP_001124457.1:n.1276+30_1276+38del
NM_001130986.2:c.1183+30_1183+38del	NP_001124458.1:n.1183+30_1183+38del
NM_003494.4:c.1180+30_1180+38del MANE Plus Clinical	NP_003485.1:n.1180+30_1180+38del