Canonical Allele Identifier: CA347223531

Gene: DYSF

Linked Data

• MyVariant Identifiers: chr2:g.71896766A>C (hg19) ; chr2:g.71669636A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71669636A>C , CM000664.2:g.71669636A>C	GRCh38
NC_000002.11:g.71896766A>C , CM000664.1:g.71896766A>C	GRCh37
NC_000002.10:g.71750274A>C	NCBI36
NG_008694.1:g.221014A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.3088A>C	ENSP00000513536.1:p.Lys1030Gln
ENST00000698058.1:c.2305A>C	ENSP00000513537.1:p.Lys769Gln
ENST00000698059.1:c.2413A>C	ENSP00000513538.1:p.Lys805Gln
ENST00000258104.8:c.5557A>C MANE Plus Clinical	ENSP00000258104.3:p.Lys1853Gln
ENST00000410020.8:c.5674A>C MANE Select	ENSP00000386881.3:p.Lys1892Gln
ENST00000258104.7:c.5557A>C	ENSP00000258104.3:p.Lys1853Gln
ENST00000394120.6:c.5560A>C	ENSP00000377678.2:p.Lys1854Gln
ENST00000409366.5:c.5623A>C	ENSP00000386512.1:p.Lys1875Gln
ENST00000409582.7:c.5671A>C	ENSP00000386547.3:p.Lys1891Gln
ENST00000409651.5:c.5653A>C	ENSP00000386683.1:p.Lys1885Gln
ENST00000409744.5:c.5581A>C	ENSP00000386285.1:p.Lys1861Gln
ENST00000409762.5:c.5608A>C	ENSP00000387137.1:p.Lys1870Gln
ENST00000410020.7:c.5674A>C	ENSP00000386881.3:p.Lys1892Gln
ENST00000410041.1:c.5611A>C	ENSP00000386617.1:p.Lys1871Gln
ENST00000413539.6:c.5650A>C	ENSP00000407046.2:p.Lys1884Gln
ENST00000429174.6:c.5620A>C	ENSP00000398305.2:p.Lys1874Gln
ENST00000479049.6:n.2442A>C
NM_001130455.1:c.5560A>C	NP_001123927.1:p.Lys1854Gln
NM_001130976.1:c.5515A>C	NP_001124448.1:p.Lys1839Gln
NM_001130977.1:c.5578A>C	NP_001124449.1:p.Lys1860Gln
NM_001130978.1:c.5620A>C	NP_001124450.1:p.Lys1874Gln
NM_001130979.1:c.5650A>C	NP_001124451.1:p.Lys1884Gln
NM_001130980.1:c.5608A>C	NP_001124452.1:p.Lys1870Gln
NM_001130981.1:c.5671A>C	NP_001124453.1:p.Lys1891Gln
NM_001130982.1:c.5653A>C	NP_001124454.1:p.Lys1885Gln
NM_001130983.1:c.5623A>C	NP_001124455.1:p.Lys1875Gln
NM_001130984.1:c.5581A>C	NP_001124456.1:p.Lys1861Gln
NM_001130985.1:c.5611A>C	NP_001124457.1:p.Lys1871Gln
NM_001130986.1:c.5518A>C	NP_001124458.1:p.Lys1840Gln
NM_001130987.1:c.5674A>C	NP_001124459.1:p.Lys1892Gln
NM_003494.3:c.5557A>C	NP_003485.1:p.Lys1853Gln
XM_005264584.3:c.5716A>C	XP_005264641.1:p.Lys1906Gln
XM_005264585.3:c.5713A>C	XP_005264642.1:p.Lys1905Gln
XM_005264584.4:c.5716A>C	XP_005264641.1:p.Lys1906Gln
XM_005264585.5:c.5713A>C	XP_005264642.1:p.Lys1905Gln
NM_001130987.2:c.5674A>C MANE Select	NP_001124459.1:p.Lys1892Gln
NM_001130455.2:c.5560A>C	NP_001123927.1:p.Lys1854Gln
NM_001130976.2:c.5515A>C	NP_001124448.1:p.Lys1839Gln
NM_001130977.2:c.5578A>C	NP_001124449.1:p.Lys1860Gln
NM_001130978.2:c.5620A>C	NP_001124450.1:p.Lys1874Gln
NM_001130979.2:c.5650A>C	NP_001124451.1:p.Lys1884Gln
NM_001130980.2:c.5608A>C	NP_001124452.1:p.Lys1870Gln
NM_001130981.2:c.5671A>C	NP_001124453.1:p.Lys1891Gln
NM_001130982.2:c.5653A>C	NP_001124454.1:p.Lys1885Gln
NM_001130983.2:c.5623A>C	NP_001124455.1:p.Lys1875Gln
NM_001130984.2:c.5581A>C	NP_001124456.1:p.Lys1861Gln
NM_001130985.2:c.5611A>C	NP_001124457.1:p.Lys1871Gln
NM_001130986.2:c.5518A>C	NP_001124458.1:p.Lys1840Gln
NM_003494.4:c.5557A>C MANE Plus Clinical	NP_003485.1:p.Lys1853Gln