Canonical Allele Identifier: CA347223174

Gene: DYSF

Linked Data

• MyVariant Identifiers: chr2:g.71896336G>C (hg19) ; chr2:g.71669206G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71669206G>C , CM000664.2:g.71669206G>C	GRCh38
NC_000002.11:g.71896336G>C , CM000664.1:g.71896336G>C	GRCh37
NC_000002.10:g.71749844G>C	NCBI36
NG_008694.1:g.220584G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.3055G>C	ENSP00000513536.1:p.Gly1019Arg
ENST00000698058.1:c.2272G>C	ENSP00000513537.1:p.Gly758Arg
ENST00000698059.1:c.2380G>C	ENSP00000513538.1:p.Gly794Arg
ENST00000258104.8:c.5524G>C MANE Plus Clinical	ENSP00000258104.3:p.Gly1842Arg
ENST00000410020.8:c.5641G>C MANE Select	ENSP00000386881.3:p.Gly1881Arg
ENST00000258104.7:c.5524G>C	ENSP00000258104.3:p.Gly1842Arg
ENST00000394120.6:c.5527G>C	ENSP00000377678.2:p.Gly1843Arg
ENST00000409366.5:c.5590G>C	ENSP00000386512.1:p.Gly1864Arg
ENST00000409582.7:c.5638G>C	ENSP00000386547.3:p.Gly1880Arg
ENST00000409651.5:c.5620G>C	ENSP00000386683.1:p.Gly1874Arg
ENST00000409744.5:c.5548G>C	ENSP00000386285.1:p.Gly1850Arg
ENST00000409762.5:c.5575G>C	ENSP00000387137.1:p.Gly1859Arg
ENST00000410020.7:c.5641G>C	ENSP00000386881.3:p.Gly1881Arg
ENST00000410041.1:c.5578G>C	ENSP00000386617.1:p.Gly1860Arg
ENST00000413539.6:c.5617G>C	ENSP00000407046.2:p.Gly1873Arg
ENST00000429174.6:c.5587G>C	ENSP00000398305.2:p.Gly1863Arg
ENST00000479049.6:n.2409G>C
NM_001130455.1:c.5527G>C	NP_001123927.1:p.Gly1843Arg
NM_001130976.1:c.5482G>C	NP_001124448.1:p.Gly1828Arg
NM_001130977.1:c.5545G>C	NP_001124449.1:p.Gly1849Arg
NM_001130978.1:c.5587G>C	NP_001124450.1:p.Gly1863Arg
NM_001130979.1:c.5617G>C	NP_001124451.1:p.Gly1873Arg
NM_001130980.1:c.5575G>C	NP_001124452.1:p.Gly1859Arg
NM_001130981.1:c.5638G>C	NP_001124453.1:p.Gly1880Arg
NM_001130982.1:c.5620G>C	NP_001124454.1:p.Gly1874Arg
NM_001130983.1:c.5590G>C	NP_001124455.1:p.Gly1864Arg
NM_001130984.1:c.5548G>C	NP_001124456.1:p.Gly1850Arg
NM_001130985.1:c.5578G>C	NP_001124457.1:p.Gly1860Arg
NM_001130986.1:c.5485G>C	NP_001124458.1:p.Gly1829Arg
NM_001130987.1:c.5641G>C	NP_001124459.1:p.Gly1881Arg
NM_003494.3:c.5524G>C	NP_003485.1:p.Gly1842Arg
XM_005264584.3:c.5683G>C	XP_005264641.1:p.Gly1895Arg
XM_005264585.3:c.5680G>C	XP_005264642.1:p.Gly1894Arg
XM_005264584.4:c.5683G>C	XP_005264641.1:p.Gly1895Arg
XM_005264585.5:c.5680G>C	XP_005264642.1:p.Gly1894Arg
NM_001130987.2:c.5641G>C MANE Select	NP_001124459.1:p.Gly1881Arg
NM_001130455.2:c.5527G>C	NP_001123927.1:p.Gly1843Arg
NM_001130976.2:c.5482G>C	NP_001124448.1:p.Gly1828Arg
NM_001130977.2:c.5545G>C	NP_001124449.1:p.Gly1849Arg
NM_001130978.2:c.5587G>C	NP_001124450.1:p.Gly1863Arg
NM_001130979.2:c.5617G>C	NP_001124451.1:p.Gly1873Arg
NM_001130980.2:c.5575G>C	NP_001124452.1:p.Gly1859Arg
NM_001130981.2:c.5638G>C	NP_001124453.1:p.Gly1880Arg
NM_001130982.2:c.5620G>C	NP_001124454.1:p.Gly1874Arg
NM_001130983.2:c.5590G>C	NP_001124455.1:p.Gly1864Arg
NM_001130984.2:c.5548G>C	NP_001124456.1:p.Gly1850Arg
NM_001130985.2:c.5578G>C	NP_001124457.1:p.Gly1860Arg
NM_001130986.2:c.5485G>C	NP_001124458.1:p.Gly1829Arg
NM_003494.4:c.5524G>C MANE Plus Clinical	NP_003485.1:p.Gly1842Arg