Canonical Allele Identifier: CA2062472544

Gene: MVK

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109595079G= , CM000674.2:g.109595079G=	GRCh38
NC_000012.11:g.110032884G= , CM000674.1:g.110032884G=	GRCh37
NC_000012.10:g.108517267G=	NCBI36
NG_007702.1:g.26385G= , LRG_156:g.26385G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000539696.6:c.94G=	ENSP00000439134.1:p.Ala32=
ENST00000546277.6:c.937G=	ENSP00000438153.2:p.Ala313=
ENST00000636529.2:n.576G=
ENST00000697195.1:c.*701G=	ENSP00000513181.1:n.*701G=
ENST00000697196.1:c.*110G=	ENSP00000513182.1:n.*110G=
ENST00000697197.1:n.2966G=
ENST00000697198.1:n.1321G=
ENST00000228510.8:c.937G= MANE Select	ENSP00000228510.3:p.Ala313=
ENST00000636529.1:c.562G=
ENST00000636996.1:c.785G=
ENST00000228510.7:c.937G=	ENSP00000228510.3:p.Ala313=
ENST00000392727.7:c.781G=	ENSP00000376487.3:p.Ala261=
ENST00000447878.6:c.*384G=	ENSP00000415555.2:n.*384G=
ENST00000537237.5:c.*610G=	ENSP00000445382.1:n.*610G=
ENST00000539575.4:c.937G=	ENSP00000443551.2:p.Ala313=
ENST00000539696.5:c.94G=	ENSP00000439134.1:p.Ala32=
ENST00000540353.1:n.3170G=
ENST00000625889.2:c.781G=	ENSP00000486846.1:p.Ala261=
ENST00000629016.2:c.*384G=	ENSP00000486804.1:n.*384G=
NM_000431.3:c.937G=	NP_000422.1:p.Ala313=
NM_001114185.2:c.937G=	NP_001107657.1:p.Ala313=
NM_001301182.1:c.781G=	NP_001288111.1:p.Ala261=
XM_011538372.1:c.937G=	XP_011536674.1:p.Ala313=
XM_017019313.2:c.781G=	XP_016874802.1:p.Ala261=
XM_017019314.1:c.937G=	XP_016874803.1:p.Ala313=
NM_000431.4:c.937G= MANE Select	NP_000422.1:p.Ala313=
NM_001114185.3:c.937G=	NP_001107657.1:p.Ala313=
NM_001301182.2:c.781G=	NP_001288111.1:p.Ala261=