Canonical Allele Identifier: CA2062437985

Gene: MVK

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109586058G= , CM000674.2:g.109586058G=	GRCh38
NC_000012.11:g.110023863G= , CM000674.1:g.110023863G=	GRCh37
NC_000012.10:g.108508246G=	NCBI36
NG_007702.1:g.17364G= , LRG_156:g.17364G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.-91-4788G=	ENSP00000439134.1:n.-91-4788G=
ENST00000546277.6:c.564G=	ENSP00000438153.2:p.Trp188=
ENST00000636529.2:n.115G=
ENST00000697195.1:c.*328G=	ENSP00000513181.1:n.*328G=
ENST00000697196.1:c.564G=	ENSP00000513182.1:p.Trp188=
ENST00000228510.8:c.564G= MANE Select	ENSP00000228510.3:p.Trp188=
ENST00000636529.1:c.101G=
ENST00000636996.1:c.412G=
ENST00000228510.7:c.564G=	ENSP00000228510.3:p.Trp188=
ENST00000392727.7:c.408G=	ENSP00000376487.3:p.Trp136=
ENST00000447878.6:c.*11G=	ENSP00000415555.2:n.*11G=
ENST00000535044.1:n.508G=
ENST00000537237.5:c.*328G=	ENSP00000445382.1:n.*328G=
ENST00000539575.4:c.564G=	ENSP00000443551.2:p.Trp188=
ENST00000539696.5:c.-91-4788G=	ENSP00000439134.1:n.-91-4788G=
ENST00000545516.1:n.109G=
ENST00000545774.5:c.*11G=	ENSP00000443978.1:n.*11G=
ENST00000546277.5:c.564G=	ENSP00000438153.1:p.Trp188=
ENST00000625889.2:c.408G=	ENSP00000486846.1:p.Trp136=
ENST00000629016.2:c.*11G=	ENSP00000486804.1:n.*11G=
NM_000431.3:c.564G=	NP_000422.1:p.Trp188=
NM_001114185.2:c.564G=	NP_001107657.1:p.Trp188=
NM_001301182.1:c.408G=	NP_001288111.1:p.Trp136=
XM_011538372.1:c.564G=	XP_011536674.1:p.Trp188=
XM_017019313.2:c.408G=	XP_016874802.1:p.Trp136=
XM_017019314.1:c.564G=	XP_016874803.1:p.Trp188=
XM_024448982.1:c.564G=	XP_024304750.1:p.Trp188=
NM_000431.4:c.564G= MANE Select	NP_000422.1:p.Trp188=
NM_001114185.3:c.564G=	NP_001107657.1:p.Trp188=
NM_001301182.2:c.408G=	NP_001288111.1:p.Trp136=