Canonical Allele Identifier: CA2062473265

Gene: MVK

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109596787C= , CM000674.2:g.109596787C=	GRCh38
NC_000012.11:g.110034592C= , CM000674.1:g.110034592C=	GRCh37
NC_000012.10:g.108518975C=	NCBI36
NG_007702.1:g.28093C= , LRG_156:g.28093C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000539696.6:c.*210C=	ENSP00000439134.1:n.*210C=
ENST00000546277.6:c.*210C=	ENSP00000438153.2:n.*210C=
ENST00000636529.2:n.1040C=
ENST00000697195.1:c.*1165C=	ENSP00000513181.1:n.*1165C=
ENST00000697196.1:c.*574C=	ENSP00000513182.1:n.*574C=
ENST00000697197.1:n.3430C=
ENST00000697198.1:n.1785C=
ENST00000228510.8:c.*210C= MANE Select	ENSP00000228510.3:n.*210C=
ENST00000636529.1:c.1026C=
ENST00000636996.1:c.1249C=
ENST00000228510.7:c.*210C=	ENSP00000228510.3:n.*210C=
ENST00000392727.7:c.*210C=	ENSP00000376487.3:n.*210C=
ENST00000447878.6:c.*848C=	ENSP00000415555.2:n.*848C=
ENST00000539575.4:c.*210C=	ENSP00000443551.2:n.*210C=
ENST00000540353.1:n.3634C=
ENST00000625889.2:c.*210C=	ENSP00000486846.1:n.*210C=
ENST00000629016.2:c.*848C=	ENSP00000486804.1:n.*848C=
NM_000431.3:c.*210C=	NP_000422.1:n.*210C=
NM_001114185.2:c.*210C=	NP_001107657.1:n.*210C=
NM_001301182.1:c.*210C=	NP_001288111.1:n.*210C=
XM_011538372.1:c.*210C=	XP_011536674.1:n.*210C=
XM_017019313.2:c.*210C=	XP_016874802.1:n.*210C=
XM_017019314.1:c.*210C=	XP_016874803.1:n.*210C=
NM_000431.4:c.*210C= MANE Select	NP_000422.1:n.*210C=
NM_001114185.3:c.*210C=	NP_001107657.1:n.*210C=
NM_001301182.2:c.*210C=	NP_001288111.1:n.*210C=