Canonical Allele Identifier: CA347223170

Gene: DYSF

Linked Data

• MyVariant Identifiers: chr2:g.71896335A>T (hg19) ; chr2:g.71669205A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71669205A>T , CM000664.2:g.71669205A>T	GRCh38
NC_000002.11:g.71896335A>T , CM000664.1:g.71896335A>T	GRCh37
NC_000002.10:g.71749843A>T	NCBI36
NG_008694.1:g.220583A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.3054A>T	ENSP00000513536.1:p.Lys1018Asn
ENST00000698058.1:c.2271A>T	ENSP00000513537.1:p.Lys757Asn
ENST00000698059.1:c.2379A>T	ENSP00000513538.1:p.Lys793Asn
ENST00000258104.8:c.5523A>T MANE Plus Clinical	ENSP00000258104.3:p.Lys1841Asn
ENST00000410020.8:c.5640A>T MANE Select	ENSP00000386881.3:p.Lys1880Asn
ENST00000258104.7:c.5523A>T	ENSP00000258104.3:p.Lys1841Asn
ENST00000394120.6:c.5526A>T	ENSP00000377678.2:p.Lys1842Asn
ENST00000409366.5:c.5589A>T	ENSP00000386512.1:p.Lys1863Asn
ENST00000409582.7:c.5637A>T	ENSP00000386547.3:p.Lys1879Asn
ENST00000409651.5:c.5619A>T	ENSP00000386683.1:p.Lys1873Asn
ENST00000409744.5:c.5547A>T	ENSP00000386285.1:p.Lys1849Asn
ENST00000409762.5:c.5574A>T	ENSP00000387137.1:p.Lys1858Asn
ENST00000410020.7:c.5640A>T	ENSP00000386881.3:p.Lys1880Asn
ENST00000410041.1:c.5577A>T	ENSP00000386617.1:p.Lys1859Asn
ENST00000413539.6:c.5616A>T	ENSP00000407046.2:p.Lys1872Asn
ENST00000429174.6:c.5586A>T	ENSP00000398305.2:p.Lys1862Asn
ENST00000479049.6:n.2408A>T
NM_001130455.1:c.5526A>T	NP_001123927.1:p.Lys1842Asn
NM_001130976.1:c.5481A>T	NP_001124448.1:p.Lys1827Asn
NM_001130977.1:c.5544A>T	NP_001124449.1:p.Lys1848Asn
NM_001130978.1:c.5586A>T	NP_001124450.1:p.Lys1862Asn
NM_001130979.1:c.5616A>T	NP_001124451.1:p.Lys1872Asn
NM_001130980.1:c.5574A>T	NP_001124452.1:p.Lys1858Asn
NM_001130981.1:c.5637A>T	NP_001124453.1:p.Lys1879Asn
NM_001130982.1:c.5619A>T	NP_001124454.1:p.Lys1873Asn
NM_001130983.1:c.5589A>T	NP_001124455.1:p.Lys1863Asn
NM_001130984.1:c.5547A>T	NP_001124456.1:p.Lys1849Asn
NM_001130985.1:c.5577A>T	NP_001124457.1:p.Lys1859Asn
NM_001130986.1:c.5484A>T	NP_001124458.1:p.Lys1828Asn
NM_001130987.1:c.5640A>T	NP_001124459.1:p.Lys1880Asn
NM_003494.3:c.5523A>T	NP_003485.1:p.Lys1841Asn
XM_005264584.3:c.5682A>T	XP_005264641.1:p.Lys1894Asn
XM_005264585.3:c.5679A>T	XP_005264642.1:p.Lys1893Asn
XM_005264584.4:c.5682A>T	XP_005264641.1:p.Lys1894Asn
XM_005264585.5:c.5679A>T	XP_005264642.1:p.Lys1893Asn
NM_001130987.2:c.5640A>T MANE Select	NP_001124459.1:p.Lys1880Asn
NM_001130455.2:c.5526A>T	NP_001123927.1:p.Lys1842Asn
NM_001130976.2:c.5481A>T	NP_001124448.1:p.Lys1827Asn
NM_001130977.2:c.5544A>T	NP_001124449.1:p.Lys1848Asn
NM_001130978.2:c.5586A>T	NP_001124450.1:p.Lys1862Asn
NM_001130979.2:c.5616A>T	NP_001124451.1:p.Lys1872Asn
NM_001130980.2:c.5574A>T	NP_001124452.1:p.Lys1858Asn
NM_001130981.2:c.5637A>T	NP_001124453.1:p.Lys1879Asn
NM_001130982.2:c.5619A>T	NP_001124454.1:p.Lys1873Asn
NM_001130983.2:c.5589A>T	NP_001124455.1:p.Lys1863Asn
NM_001130984.2:c.5547A>T	NP_001124456.1:p.Lys1849Asn
NM_001130985.2:c.5577A>T	NP_001124457.1:p.Lys1859Asn
NM_001130986.2:c.5484A>T	NP_001124458.1:p.Lys1828Asn
NM_003494.4:c.5523A>T MANE Plus Clinical	NP_003485.1:p.Lys1841Asn