Canonical Allele Identifier: CA2062473151

Gene: MVK

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109596598G= , CM000674.2:g.109596598G=	GRCh38
NC_000012.11:g.110034403G= , CM000674.1:g.110034403G=	GRCh37
NC_000012.10:g.108518786G=	NCBI36
NG_007702.1:g.27904G= , LRG_156:g.27904G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.*21G=	ENSP00000439134.1:n.*21G=
ENST00000546277.6:c.*21G=	ENSP00000438153.2:n.*21G=
ENST00000636529.2:n.851G=
ENST00000697195.1:c.*976G=	ENSP00000513181.1:n.*976G=
ENST00000697196.1:c.*385G=	ENSP00000513182.1:n.*385G=
ENST00000697197.1:n.3241G=
ENST00000697198.1:n.1596G=
ENST00000228510.8:c.*21G= MANE Select	ENSP00000228510.3:n.*21G=
ENST00000636529.1:c.837G=
ENST00000636996.1:c.1060G=
ENST00000228510.7:c.*21G=	ENSP00000228510.3:n.*21G=
ENST00000392727.7:c.*21G=	ENSP00000376487.3:n.*21G=
ENST00000447878.6:c.*659G=	ENSP00000415555.2:n.*659G=
ENST00000539575.4:c.*21G=	ENSP00000443551.2:n.*21G=
ENST00000539696.5:c.*21G=	ENSP00000439134.1:n.*21G=
ENST00000540353.1:n.3445G=
ENST00000625889.2:c.*21G=	ENSP00000486846.1:n.*21G=
ENST00000629016.2:c.*659G=	ENSP00000486804.1:n.*659G=
NM_000431.3:c.*21G=	NP_000422.1:n.*21G=
NM_001114185.2:c.*21G=	NP_001107657.1:n.*21G=
NM_001301182.1:c.*21G=	NP_001288111.1:n.*21G=
XM_011538372.1:c.*21G=	XP_011536674.1:n.*21G=
XM_017019313.2:c.*21G=	XP_016874802.1:n.*21G=
XM_017019314.1:c.*21G=	XP_016874803.1:n.*21G=
NM_000431.4:c.*21G= MANE Select	NP_000422.1:n.*21G=
NM_001114185.3:c.*21G=	NP_001107657.1:n.*21G=
NM_001301182.2:c.*21G=	NP_001288111.1:n.*21G=