Canonical Allele Identifier: CA347217854

Gene: DYSF

Linked Data

• MyVariant Identifiers: chr2:g.71871118G>C (hg19) ; chr2:g.71643988G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71643988G>C , CM000664.2:g.71643988G>C	GRCh38
NC_000002.11:g.71871118G>C , CM000664.1:g.71871118G>C	GRCh37
NC_000002.10:g.71724626G>C	NCBI36
NG_008694.1:g.195366G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.1965G>C	ENSP00000513536.1:p.Trp655Cys
ENST00000698058.1:c.1182G>C	ENSP00000513537.1:p.Trp394Cys
ENST00000698059.1:c.1290G>C	ENSP00000513538.1:p.Trp430Cys
ENST00000258104.8:c.4434G>C MANE Plus Clinical	ENSP00000258104.3:p.Trp1478Cys
ENST00000410020.8:c.4551G>C MANE Select	ENSP00000386881.3:p.Trp1517Cys
ENST00000258104.7:c.4434G>C	ENSP00000258104.3:p.Trp1478Cys
ENST00000394120.6:c.4437G>C	ENSP00000377678.2:p.Trp1479Cys
ENST00000409366.5:c.4500G>C	ENSP00000386512.1:p.Trp1500Cys
ENST00000409582.7:c.4548G>C	ENSP00000386547.3:p.Trp1516Cys
ENST00000409651.5:c.4530G>C	ENSP00000386683.1:p.Trp1510Cys
ENST00000409744.5:c.4458G>C	ENSP00000386285.1:p.Trp1486Cys
ENST00000409762.5:c.4485G>C	ENSP00000387137.1:p.Trp1495Cys
ENST00000410020.7:c.4551G>C	ENSP00000386881.3:p.Trp1517Cys
ENST00000410041.1:c.4488G>C	ENSP00000386617.1:p.Trp1496Cys
ENST00000413539.6:c.4527G>C	ENSP00000407046.2:p.Trp1509Cys
ENST00000429174.6:c.4497G>C	ENSP00000398305.2:p.Trp1499Cys
ENST00000468173.1:n.733G>C
ENST00000479049.6:n.1319G>C
NM_001130455.1:c.4437G>C	NP_001123927.1:p.Trp1479Cys
NM_001130976.1:c.4392G>C	NP_001124448.1:p.Trp1464Cys
NM_001130977.1:c.4455G>C	NP_001124449.1:p.Trp1485Cys
NM_001130978.1:c.4497G>C	NP_001124450.1:p.Trp1499Cys
NM_001130979.1:c.4527G>C	NP_001124451.1:p.Trp1509Cys
NM_001130980.1:c.4485G>C	NP_001124452.1:p.Trp1495Cys
NM_001130981.1:c.4548G>C	NP_001124453.1:p.Trp1516Cys
NM_001130982.1:c.4530G>C	NP_001124454.1:p.Trp1510Cys
NM_001130983.1:c.4500G>C	NP_001124455.1:p.Trp1500Cys
NM_001130984.1:c.4458G>C	NP_001124456.1:p.Trp1486Cys
NM_001130985.1:c.4488G>C	NP_001124457.1:p.Trp1496Cys
NM_001130986.1:c.4395G>C	NP_001124458.1:p.Trp1465Cys
NM_001130987.1:c.4551G>C	NP_001124459.1:p.Trp1517Cys
NM_003494.3:c.4434G>C	NP_003485.1:p.Trp1478Cys
XM_005264584.3:c.4593G>C	XP_005264641.1:p.Trp1531Cys
XM_005264585.3:c.4590G>C	XP_005264642.1:p.Trp1530Cys
XM_005264584.4:c.4593G>C	XP_005264641.1:p.Trp1531Cys
XM_005264585.5:c.4590G>C	XP_005264642.1:p.Trp1530Cys
XR_001738969.1:n.4751G>C
NM_001130987.2:c.4551G>C MANE Select	NP_001124459.1:p.Trp1517Cys
NM_001130455.2:c.4437G>C	NP_001123927.1:p.Trp1479Cys
NM_001130976.2:c.4392G>C	NP_001124448.1:p.Trp1464Cys
NM_001130977.2:c.4455G>C	NP_001124449.1:p.Trp1485Cys
NM_001130978.2:c.4497G>C	NP_001124450.1:p.Trp1499Cys
NM_001130979.2:c.4527G>C	NP_001124451.1:p.Trp1509Cys
NM_001130980.2:c.4485G>C	NP_001124452.1:p.Trp1495Cys
NM_001130981.2:c.4548G>C	NP_001124453.1:p.Trp1516Cys
NM_001130982.2:c.4530G>C	NP_001124454.1:p.Trp1510Cys
NM_001130983.2:c.4500G>C	NP_001124455.1:p.Trp1500Cys
NM_001130984.2:c.4458G>C	NP_001124456.1:p.Trp1486Cys
NM_001130985.2:c.4488G>C	NP_001124457.1:p.Trp1496Cys
NM_001130986.2:c.4395G>C	NP_001124458.1:p.Trp1465Cys
NM_003494.4:c.4434G>C MANE Plus Clinical	NP_003485.1:p.Trp1478Cys