Canonical Allele Identifier: CA49740952
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 94287
ClinVar RCV Id: RCV000594361
dbSNP Id: rs398123774

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71561941_71561945del , CM000664.2:g.71561941_71561945del GRCh38
NC_000002.11:g.71789071_71789075del , CM000664.1:g.71789071_71789075del GRCh37
NC_000002.10:g.71642579_71642583del NCBI36
NG_008694.1:g.113319_113323del

Transcript Alleles

HGVS Amino-acid change
ENST00000258104.8:c.2352_2355+1del
ENST00000410020.8:c.2406_2409+1del
ENST00000258104.7:c.2352_2355+1del
ENST00000394120.6:c.2355_2358+1del
ENST00000409366.5:c.2355_2358+1del
ENST00000409582.7:c.2403_2406+1del
ENST00000409651.5:c.2448_2451+1del
ENST00000409744.5:c.2313_2316+1del
ENST00000409762.5:c.2403_2406+1del
ENST00000410020.7:c.2406_2409+1del
ENST00000410041.1:c.2406_2409+1del
ENST00000413539.6:c.2445_2448+1del
ENST00000429174.6:c.2352_2355+1del
NM_001130455.1:c.2355_2358+1del
NM_001130976.1:c.2310_2313+1del
NM_001130977.1:c.2310_2313+1del
NM_001130978.1:c.2352_2355+1del
NM_001130979.1:c.2445_2448+1del
NM_001130980.1:c.2403_2406+1del
NM_001130981.1:c.2403_2406+1del
NM_001130982.1:c.2448_2451+1del
NM_001130983.1:c.2355_2358+1del
NM_001130984.1:c.2313_2316+1del
NM_001130985.1:c.2406_2409+1del
NM_001130986.1:c.2313_2316+1del
NM_001130987.1:c.2406_2409+1del
NM_003494.3:c.2352_2355+1del
XM_005264584.3:c.2448_2451+1del
XM_005264585.3:c.2445_2448+1del
XM_005264584.4:c.2448_2451+1del
XM_005264585.5:c.2445_2448+1del
XR_001738969.1:n.2606_2609+1del
NM_001130987.2:c.2406_2409+1del
NM_001130455.2:c.2355_2358+1del
NM_001130976.2:c.2310_2313+1del
NM_001130977.2:c.2310_2313+1del
NM_001130978.2:c.2352_2355+1del
NM_001130979.2:c.2445_2448+1del
NM_001130980.2:c.2403_2406+1del
NM_001130981.2:c.2403_2406+1del
NM_001130982.2:c.2448_2451+1del
NM_001130983.2:c.2355_2358+1del
NM_001130984.2:c.2313_2316+1del
NM_001130985.2:c.2406_2409+1del
NM_001130986.2:c.2313_2316+1del
NM_003494.4:c.2352_2355+1del