Canonical Allele Identifier: CA347226474

Gene: DYSF

Linked Data

• MyVariant Identifiers: chr2:g.71906307A>T (hg19) ; chr2:g.71679177A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71679177A>T , CM000664.2:g.71679177A>T	GRCh38
NC_000002.11:g.71906307A>T , CM000664.1:g.71906307A>T	GRCh37
NC_000002.10:g.71759815A>T	NCBI36
NG_008694.1:g.230555A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000698057.1:c.3419A>T	ENSP00000513536.1:p.Lys1140Ile
ENST00000698058.1:c.2636A>T	ENSP00000513537.1:p.Lys879Ile
ENST00000698059.1:c.2744A>T	ENSP00000513538.1:p.Lys915Ile
ENST00000258104.8:c.5888A>T MANE Plus Clinical	ENSP00000258104.3:p.Lys1963Ile
ENST00000410020.8:c.6005A>T MANE Select	ENSP00000386881.3:p.Lys2002Ile
ENST00000258104.7:c.5888A>T	ENSP00000258104.3:p.Lys1963Ile
ENST00000394120.6:c.5891A>T	ENSP00000377678.2:p.Lys1964Ile
ENST00000409366.5:c.5954A>T	ENSP00000386512.1:p.Lys1985Ile
ENST00000409582.7:c.6002A>T	ENSP00000386547.3:p.Lys2001Ile
ENST00000409651.5:c.5984A>T	ENSP00000386683.1:p.Lys1995Ile
ENST00000409744.5:c.5912A>T	ENSP00000386285.1:p.Lys1971Ile
ENST00000409762.5:c.5939A>T	ENSP00000387137.1:p.Lys1980Ile
ENST00000410020.7:c.6005A>T	ENSP00000386881.3:p.Lys2002Ile
ENST00000410041.1:c.5942A>T	ENSP00000386617.1:p.Lys1981Ile
ENST00000413539.6:c.5981A>T	ENSP00000407046.2:p.Lys1994Ile
ENST00000429174.6:c.5951A>T	ENSP00000398305.2:p.Lys1984Ile
ENST00000479049.6:n.2773A>T
NM_001130455.1:c.5891A>T	NP_001123927.1:p.Lys1964Ile
NM_001130976.1:c.5846A>T	NP_001124448.1:p.Lys1949Ile
NM_001130977.1:c.5909A>T	NP_001124449.1:p.Lys1970Ile
NM_001130978.1:c.5951A>T	NP_001124450.1:p.Lys1984Ile
NM_001130979.1:c.5981A>T	NP_001124451.1:p.Lys1994Ile
NM_001130980.1:c.5939A>T	NP_001124452.1:p.Lys1980Ile
NM_001130981.1:c.6002A>T	NP_001124453.1:p.Lys2001Ile
NM_001130982.1:c.5984A>T	NP_001124454.1:p.Lys1995Ile
NM_001130983.1:c.5954A>T	NP_001124455.1:p.Lys1985Ile
NM_001130984.1:c.5912A>T	NP_001124456.1:p.Lys1971Ile
NM_001130985.1:c.5942A>T	NP_001124457.1:p.Lys1981Ile
NM_001130986.1:c.5849A>T	NP_001124458.1:p.Lys1950Ile
NM_001130987.1:c.6005A>T	NP_001124459.1:p.Lys2002Ile
NM_003494.3:c.5888A>T	NP_003485.1:p.Lys1963Ile
XM_005264584.3:c.6047A>T	XP_005264641.1:p.Lys2016Ile
XM_005264585.3:c.6044A>T	XP_005264642.1:p.Lys2015Ile
XM_005264584.4:c.6047A>T	XP_005264641.1:p.Lys2016Ile
XM_005264585.5:c.6044A>T	XP_005264642.1:p.Lys2015Ile
NM_001130987.2:c.6005A>T MANE Select	NP_001124459.1:p.Lys2002Ile
NM_001130455.2:c.5891A>T	NP_001123927.1:p.Lys1964Ile
NM_001130976.2:c.5846A>T	NP_001124448.1:p.Lys1949Ile
NM_001130977.2:c.5909A>T	NP_001124449.1:p.Lys1970Ile
NM_001130978.2:c.5951A>T	NP_001124450.1:p.Lys1984Ile
NM_001130979.2:c.5981A>T	NP_001124451.1:p.Lys1994Ile
NM_001130980.2:c.5939A>T	NP_001124452.1:p.Lys1980Ile
NM_001130981.2:c.6002A>T	NP_001124453.1:p.Lys2001Ile
NM_001130982.2:c.5984A>T	NP_001124454.1:p.Lys1995Ile
NM_001130983.2:c.5954A>T	NP_001124455.1:p.Lys1985Ile
NM_001130984.2:c.5912A>T	NP_001124456.1:p.Lys1971Ile
NM_001130985.2:c.5942A>T	NP_001124457.1:p.Lys1981Ile
NM_001130986.2:c.5849A>T	NP_001124458.1:p.Lys1950Ile
NM_003494.4:c.5888A>T MANE Plus Clinical	NP_003485.1:p.Lys1963Ile