Canonical Allele Identifier: CA2062473304

Gene: MVK

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109596890G= , CM000674.2:g.109596890G=	GRCh38
NC_000012.11:g.110034695G= , CM000674.1:g.110034695G=	GRCh37
NC_000012.10:g.108519078G=	NCBI36
NG_007702.1:g.28196G= , LRG_156:g.28196G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.*313G=	ENSP00000439134.1:n.*313G=
ENST00000546277.6:c.*313G=	ENSP00000438153.2:n.*313G=
ENST00000636529.2:n.1143G=
ENST00000697195.1:c.*1268G=	ENSP00000513181.1:n.*1268G=
ENST00000697196.1:c.*677G=	ENSP00000513182.1:n.*677G=
ENST00000697197.1:n.3533G=
ENST00000697198.1:n.1888G=
ENST00000228510.8:c.*313G= MANE Select	ENSP00000228510.3:n.*313G=
ENST00000636529.1:c.1129G=
ENST00000636996.1:c.1352G=
ENST00000228510.7:c.*313G=	ENSP00000228510.3:n.*313G=
ENST00000392727.7:c.*313G=	ENSP00000376487.3:n.*313G=
ENST00000447878.6:c.*951G=	ENSP00000415555.2:n.*951G=
ENST00000539575.4:c.*313G=	ENSP00000443551.2:n.*313G=
ENST00000540353.1:n.3737G=
ENST00000625889.2:c.*313G=	ENSP00000486846.1:n.*313G=
ENST00000629016.2:c.*951G=	ENSP00000486804.1:n.*951G=
NM_000431.3:c.*313G=	NP_000422.1:n.*313G=
NM_001114185.2:c.*313G=	NP_001107657.1:n.*313G=
NM_001301182.1:c.*313G=	NP_001288111.1:n.*313G=
XM_011538372.1:c.*313G=	XP_011536674.1:n.*313G=
XM_017019313.2:c.*313G=	XP_016874802.1:n.*313G=
XM_017019314.1:c.*313G=	XP_016874803.1:n.*313G=
NM_000431.4:c.*313G= MANE Select	NP_000422.1:n.*313G=
NM_001114185.3:c.*313G=	NP_001107657.1:n.*313G=
NM_001301182.2:c.*313G=	NP_001288111.1:n.*313G=