Canonical Allele Identifier: CA347223572

Gene: DYSF

Linked Data

• ClinVar Variation Id: 471318
• ClinVar RCV Id: RCV000534201
• dbSNP Id: rs1553416071
• MyVariant Identifiers: chr2:g.71896773A>T (hg19) ; chr2:g.71669643A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71669643A>T , CM000664.2:g.71669643A>T	GRCh38
NC_000002.11:g.71896773A>T , CM000664.1:g.71896773A>T	GRCh37
NC_000002.10:g.71750281A>T	NCBI36
NG_008694.1:g.221021A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.3095A>T	ENSP00000513536.1:p.Asp1032Val
ENST00000698058.1:c.2312A>T	ENSP00000513537.1:p.Asp771Val
ENST00000698059.1:c.2420A>T	ENSP00000513538.1:p.Asp807Val
ENST00000258104.8:c.5564A>T MANE Plus Clinical	ENSP00000258104.3:p.Asp1855Val
ENST00000410020.8:c.5681A>T MANE Select	ENSP00000386881.3:p.Asp1894Val
ENST00000258104.7:c.5564A>T	ENSP00000258104.3:p.Asp1855Val
ENST00000394120.6:c.5567A>T	ENSP00000377678.2:p.Asp1856Val
ENST00000409366.5:c.5630A>T	ENSP00000386512.1:p.Asp1877Val
ENST00000409582.7:c.5678A>T	ENSP00000386547.3:p.Asp1893Val
ENST00000409651.5:c.5660A>T	ENSP00000386683.1:p.Asp1887Val
ENST00000409744.5:c.5588A>T	ENSP00000386285.1:p.Asp1863Val
ENST00000409762.5:c.5615A>T	ENSP00000387137.1:p.Asp1872Val
ENST00000410020.7:c.5681A>T	ENSP00000386881.3:p.Asp1894Val
ENST00000410041.1:c.5618A>T	ENSP00000386617.1:p.Asp1873Val
ENST00000413539.6:c.5657A>T	ENSP00000407046.2:p.Asp1886Val
ENST00000429174.6:c.5627A>T	ENSP00000398305.2:p.Asp1876Val
ENST00000479049.6:n.2449A>T
NM_001130455.1:c.5567A>T	NP_001123927.1:p.Asp1856Val
NM_001130976.1:c.5522A>T	NP_001124448.1:p.Asp1841Val
NM_001130977.1:c.5585A>T	NP_001124449.1:p.Asp1862Val
NM_001130978.1:c.5627A>T	NP_001124450.1:p.Asp1876Val
NM_001130979.1:c.5657A>T	NP_001124451.1:p.Asp1886Val
NM_001130980.1:c.5615A>T	NP_001124452.1:p.Asp1872Val
NM_001130981.1:c.5678A>T	NP_001124453.1:p.Asp1893Val
NM_001130982.1:c.5660A>T	NP_001124454.1:p.Asp1887Val
NM_001130983.1:c.5630A>T	NP_001124455.1:p.Asp1877Val
NM_001130984.1:c.5588A>T	NP_001124456.1:p.Asp1863Val
NM_001130985.1:c.5618A>T	NP_001124457.1:p.Asp1873Val
NM_001130986.1:c.5525A>T	NP_001124458.1:p.Asp1842Val
NM_001130987.1:c.5681A>T	NP_001124459.1:p.Asp1894Val
NM_003494.3:c.5564A>T	NP_003485.1:p.Asp1855Val
XM_005264584.3:c.5723A>T	XP_005264641.1:p.Asp1908Val
XM_005264585.3:c.5720A>T	XP_005264642.1:p.Asp1907Val
XM_005264584.4:c.5723A>T	XP_005264641.1:p.Asp1908Val
XM_005264585.5:c.5720A>T	XP_005264642.1:p.Asp1907Val
NM_001130987.2:c.5681A>T MANE Select	NP_001124459.1:p.Asp1894Val
NM_001130455.2:c.5567A>T	NP_001123927.1:p.Asp1856Val
NM_001130976.2:c.5522A>T	NP_001124448.1:p.Asp1841Val
NM_001130977.2:c.5585A>T	NP_001124449.1:p.Asp1862Val
NM_001130978.2:c.5627A>T	NP_001124450.1:p.Asp1876Val
NM_001130979.2:c.5657A>T	NP_001124451.1:p.Asp1886Val
NM_001130980.2:c.5615A>T	NP_001124452.1:p.Asp1872Val
NM_001130981.2:c.5678A>T	NP_001124453.1:p.Asp1893Val
NM_001130982.2:c.5660A>T	NP_001124454.1:p.Asp1887Val
NM_001130983.2:c.5630A>T	NP_001124455.1:p.Asp1877Val
NM_001130984.2:c.5588A>T	NP_001124456.1:p.Asp1863Val
NM_001130985.2:c.5618A>T	NP_001124457.1:p.Asp1873Val
NM_001130986.2:c.5525A>T	NP_001124458.1:p.Asp1842Val
NM_003494.4:c.5564A>T MANE Plus Clinical	NP_003485.1:p.Asp1855Val