Canonical Allele Identifier: CA2062444587

Gene: MVK

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109591334C= , CM000674.2:g.109591334C=	GRCh38
NC_000012.11:g.110029139C= , CM000674.1:g.110029139C=	GRCh37
NC_000012.10:g.108513522C=	NCBI36
NG_007702.1:g.22640C= , LRG_156:g.22640C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.19C=	ENSP00000439134.1:p.Pro7=
ENST00000546277.6:c.862C=	ENSP00000438153.2:p.Pro288=
ENST00000636529.2:n.501C=
ENST00000697195.1:c.*626C=	ENSP00000513181.1:n.*626C=
ENST00000697196.1:c.*35C=	ENSP00000513182.1:n.*35C=
ENST00000697197.1:n.2891C=
ENST00000228510.8:c.862C= MANE Select	ENSP00000228510.3:p.Pro288=
ENST00000636529.1:c.487C=
ENST00000636996.1:c.710C=
ENST00000228510.7:c.862C=	ENSP00000228510.3:p.Pro288=
ENST00000392727.7:c.706C=	ENSP00000376487.3:p.Pro236=
ENST00000447878.6:c.*309C=	ENSP00000415555.2:n.*309C=
ENST00000537237.5:c.*535C=	ENSP00000445382.1:n.*535C=
ENST00000539575.4:c.862C=	ENSP00000443551.2:p.Pro288=
ENST00000539696.5:c.19C=	ENSP00000439134.1:p.Pro7=
ENST00000540353.1:n.3095C=
ENST00000625889.2:c.706C=	ENSP00000486846.1:p.Pro236=
ENST00000629016.2:c.*309C=	ENSP00000486804.1:n.*309C=
NM_000431.3:c.862C=	NP_000422.1:p.Pro288=
NM_001114185.2:c.862C=	NP_001107657.1:p.Pro288=
NM_001301182.1:c.706C=	NP_001288111.1:p.Pro236=
XM_011538372.1:c.862C=	XP_011536674.1:p.Pro288=
XM_017019313.2:c.706C=	XP_016874802.1:p.Pro236=
XM_017019314.1:c.862C=	XP_016874803.1:p.Pro288=
XM_024448982.1:c.862C=	XP_024304750.1:p.Pro288=
NM_000431.4:c.862C= MANE Select	NP_000422.1:p.Pro288=
NM_001114185.3:c.862C=	NP_001107657.1:p.Pro288=
NM_001301182.2:c.706C=	NP_001288111.1:p.Pro236=