Canonical Allele Identifier: CA347220500

Gene: DYSF

Linked Data

• MyVariant Identifiers: chr2:g.71891512G>T (hg19) ; chr2:g.71664382G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71664382G>T , CM000664.2:g.71664382G>T	GRCh38
NC_000002.11:g.71891512G>T , CM000664.1:g.71891512G>T	GRCh37
NC_000002.10:g.71745020G>T	NCBI36
NG_008694.1:g.215760G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.2532G>T	ENSP00000513536.1:p.Glu844Asp
ENST00000698058.1:c.1749G>T	ENSP00000513537.1:p.Glu583Asp
ENST00000698059.1:c.1857G>T	ENSP00000513538.1:p.Glu619Asp
ENST00000258104.8:c.5001G>T MANE Plus Clinical	ENSP00000258104.3:p.Glu1667Asp
ENST00000410020.8:c.5118G>T MANE Select	ENSP00000386881.3:p.Glu1706Asp
ENST00000258104.7:c.5001G>T	ENSP00000258104.3:p.Glu1667Asp
ENST00000394120.6:c.5004G>T	ENSP00000377678.2:p.Glu1668Asp
ENST00000409366.5:c.5067G>T	ENSP00000386512.1:p.Glu1689Asp
ENST00000409582.7:c.5115G>T	ENSP00000386547.3:p.Glu1705Asp
ENST00000409651.5:c.5097G>T	ENSP00000386683.1:p.Glu1699Asp
ENST00000409744.5:c.5025G>T	ENSP00000386285.1:p.Glu1675Asp
ENST00000409762.5:c.5052G>T	ENSP00000387137.1:p.Glu1684Asp
ENST00000410020.7:c.5118G>T	ENSP00000386881.3:p.Glu1706Asp
ENST00000410041.1:c.5055G>T	ENSP00000386617.1:p.Glu1685Asp
ENST00000413539.6:c.5094G>T	ENSP00000407046.2:p.Glu1698Asp
ENST00000429174.6:c.5064G>T	ENSP00000398305.2:p.Glu1688Asp
ENST00000479049.6:n.1886G>T
NM_001130455.1:c.5004G>T	NP_001123927.1:p.Glu1668Asp
NM_001130976.1:c.4959G>T	NP_001124448.1:p.Glu1653Asp
NM_001130977.1:c.5022G>T	NP_001124449.1:p.Glu1674Asp
NM_001130978.1:c.5064G>T	NP_001124450.1:p.Glu1688Asp
NM_001130979.1:c.5094G>T	NP_001124451.1:p.Glu1698Asp
NM_001130980.1:c.5052G>T	NP_001124452.1:p.Glu1684Asp
NM_001130981.1:c.5115G>T	NP_001124453.1:p.Glu1705Asp
NM_001130982.1:c.5097G>T	NP_001124454.1:p.Glu1699Asp
NM_001130983.1:c.5067G>T	NP_001124455.1:p.Glu1689Asp
NM_001130984.1:c.5025G>T	NP_001124456.1:p.Glu1675Asp
NM_001130985.1:c.5055G>T	NP_001124457.1:p.Glu1685Asp
NM_001130986.1:c.4962G>T	NP_001124458.1:p.Glu1654Asp
NM_001130987.1:c.5118G>T	NP_001124459.1:p.Glu1706Asp
NM_003494.3:c.5001G>T	NP_003485.1:p.Glu1667Asp
XM_005264584.3:c.5160G>T	XP_005264641.1:p.Glu1720Asp
XM_005264585.3:c.5157G>T	XP_005264642.1:p.Glu1719Asp
XM_005264584.4:c.5160G>T	XP_005264641.1:p.Glu1720Asp
XM_005264585.5:c.5157G>T	XP_005264642.1:p.Glu1719Asp
XR_001738969.1:n.5318G>T
NM_001130987.2:c.5118G>T MANE Select	NP_001124459.1:p.Glu1706Asp
NM_001130455.2:c.5004G>T	NP_001123927.1:p.Glu1668Asp
NM_001130976.2:c.4959G>T	NP_001124448.1:p.Glu1653Asp
NM_001130977.2:c.5022G>T	NP_001124449.1:p.Glu1674Asp
NM_001130978.2:c.5064G>T	NP_001124450.1:p.Glu1688Asp
NM_001130979.2:c.5094G>T	NP_001124451.1:p.Glu1698Asp
NM_001130980.2:c.5052G>T	NP_001124452.1:p.Glu1684Asp
NM_001130981.2:c.5115G>T	NP_001124453.1:p.Glu1705Asp
NM_001130982.2:c.5097G>T	NP_001124454.1:p.Glu1699Asp
NM_001130983.2:c.5067G>T	NP_001124455.1:p.Glu1689Asp
NM_001130984.2:c.5025G>T	NP_001124456.1:p.Glu1675Asp
NM_001130985.2:c.5055G>T	NP_001124457.1:p.Glu1685Asp
NM_001130986.2:c.4962G>T	NP_001124458.1:p.Glu1654Asp
NM_003494.4:c.5001G>T MANE Plus Clinical	NP_003485.1:p.Glu1667Asp