Canonical Allele Identifier: CA1706807

Gene: DYSF

Linked Data

• dbSNP Id: rs781449138
• ExAC: 2:71829935 G / C
• gnomAD v2: 2-71829935-G-C
• gnomAD v3: 2-71602805-G-C
• gnomAD v4: 2-71602805-G-C
• MyVariant Identifiers: chr2:g.71829935G>C (hg19) ; chr2:g.71602805G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71602805G>C , CM000664.2:g.71602805G>C	GRCh38
NC_000002.11:g.71829935G>C , CM000664.1:g.71829935G>C	GRCh37
NC_000002.10:g.71683443G>C	NCBI36
NG_008694.1:g.154183G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.1329G>C	ENSP00000513536.1:p.Glu443Asp
ENST00000698058.1:c.546G>C	ENSP00000513537.1:p.Glu182Asp
ENST00000698059.1:c.546G>C	ENSP00000513538.1:p.Glu182Asp
ENST00000258104.8:c.3903G>C MANE Plus Clinical	ENSP00000258104.3:p.Glu1301Asp
ENST00000410020.8:c.3957G>C MANE Select	ENSP00000386881.3:p.Glu1319Asp
ENST00000258104.7:c.3903G>C	ENSP00000258104.3:p.Glu1301Asp
ENST00000394120.6:c.3906G>C	ENSP00000377678.2:p.Glu1302Asp
ENST00000409366.5:c.3906G>C	ENSP00000386512.1:p.Glu1302Asp
ENST00000409582.7:c.3954G>C	ENSP00000386547.3:p.Glu1318Asp
ENST00000409651.5:c.3999G>C	ENSP00000386683.1:p.Glu1333Asp
ENST00000409744.5:c.3864G>C	ENSP00000386285.1:p.Glu1288Asp
ENST00000409762.5:c.3954G>C	ENSP00000387137.1:p.Glu1318Asp
ENST00000410020.7:c.3957G>C	ENSP00000386881.3:p.Glu1319Asp
ENST00000410041.1:c.3957G>C	ENSP00000386617.1:p.Glu1319Asp
ENST00000413539.6:c.3996G>C	ENSP00000407046.2:p.Glu1332Asp
ENST00000429174.6:c.3903G>C	ENSP00000398305.2:p.Glu1301Asp
ENST00000472873.5:n.287G>C
ENST00000479049.6:n.788G>C
ENST00000487180.5:n.122G>C
ENST00000494501.5:n.263G>C
NM_001130455.1:c.3906G>C	NP_001123927.1:p.Glu1302Asp
NM_001130976.1:c.3861G>C	NP_001124448.1:p.Glu1287Asp
NM_001130977.1:c.3861G>C	NP_001124449.1:p.Glu1287Asp
NM_001130978.1:c.3903G>C	NP_001124450.1:p.Glu1301Asp
NM_001130979.1:c.3996G>C	NP_001124451.1:p.Glu1332Asp
NM_001130980.1:c.3954G>C	NP_001124452.1:p.Glu1318Asp
NM_001130981.1:c.3954G>C	NP_001124453.1:p.Glu1318Asp
NM_001130982.1:c.3999G>C	NP_001124454.1:p.Glu1333Asp
NM_001130983.1:c.3906G>C	NP_001124455.1:p.Glu1302Asp
NM_001130984.1:c.3864G>C	NP_001124456.1:p.Glu1288Asp
NM_001130985.1:c.3957G>C	NP_001124457.1:p.Glu1319Asp
NM_001130986.1:c.3864G>C	NP_001124458.1:p.Glu1288Asp
NM_001130987.1:c.3957G>C	NP_001124459.1:p.Glu1319Asp
NM_003494.3:c.3903G>C	NP_003485.1:p.Glu1301Asp
XM_005264584.3:c.3999G>C	XP_005264641.1:p.Glu1333Asp
XM_005264585.3:c.3996G>C	XP_005264642.1:p.Glu1332Asp
XM_005264584.4:c.3999G>C	XP_005264641.1:p.Glu1333Asp
XM_005264585.5:c.3996G>C	XP_005264642.1:p.Glu1332Asp
XR_001738969.1:n.4157G>C
NM_001130987.2:c.3957G>C MANE Select	NP_001124459.1:p.Glu1319Asp
NM_001130455.2:c.3906G>C	NP_001123927.1:p.Glu1302Asp
NM_001130976.2:c.3861G>C	NP_001124448.1:p.Glu1287Asp
NM_001130977.2:c.3861G>C	NP_001124449.1:p.Glu1287Asp
NM_001130978.2:c.3903G>C	NP_001124450.1:p.Glu1301Asp
NM_001130979.2:c.3996G>C	NP_001124451.1:p.Glu1332Asp
NM_001130980.2:c.3954G>C	NP_001124452.1:p.Glu1318Asp
NM_001130981.2:c.3954G>C	NP_001124453.1:p.Glu1318Asp
NM_001130982.2:c.3999G>C	NP_001124454.1:p.Glu1333Asp
NM_001130983.2:c.3906G>C	NP_001124455.1:p.Glu1302Asp
NM_001130984.2:c.3864G>C	NP_001124456.1:p.Glu1288Asp
NM_001130985.2:c.3957G>C	NP_001124457.1:p.Glu1319Asp
NM_001130986.2:c.3864G>C	NP_001124458.1:p.Glu1288Asp
NM_003494.4:c.3903G>C MANE Plus Clinical	NP_003485.1:p.Glu1301Asp