Canonical Allele Identifier: CA386649252

Gene: MVK

Linked Data

• MyVariant Identifiers: chr12:g.110029059T>C (hg19) ; chr12:g.109591254T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109591254T>C , CM000674.2:g.109591254T>C	GRCh38
NC_000012.11:g.110029059T>C , CM000674.1:g.110029059T>C	GRCh37
NC_000012.10:g.108513442T>C	NCBI36
NG_007702.1:g.22560T>C , LRG_156:g.22560T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.-62T>C	ENSP00000439134.1:n.-62T>C
ENST00000546277.6:c.782T>C	ENSP00000438153.2:p.Val261Ala
ENST00000636529.2:n.421T>C
ENST00000697195.1:c.*546T>C	ENSP00000513181.1:n.*546T>C
ENST00000697196.1:c.870T>C	ENSP00000513182.1:p.Arg290=
ENST00000697197.1:n.2811T>C
ENST00000228510.8:c.782T>C MANE Select	ENSP00000228510.3:p.Val261Ala
ENST00000636529.1:c.407T>C
ENST00000636996.1:c.630T>C
ENST00000228510.7:c.782T>C	ENSP00000228510.3:p.Val261Ala
ENST00000392727.7:c.626T>C	ENSP00000376487.3:p.Val209Ala
ENST00000447878.6:c.*229T>C	ENSP00000415555.2:n.*229T>C
ENST00000537237.5:c.*455T>C	ENSP00000445382.1:n.*455T>C
ENST00000539575.4:c.782T>C	ENSP00000443551.2:p.Val261Ala
ENST00000539696.5:c.-62T>C	ENSP00000439134.1:n.-62T>C
ENST00000540353.1:n.3015T>C
ENST00000625889.2:c.626T>C	ENSP00000486846.1:p.Val209Ala
ENST00000629016.2:c.*229T>C	ENSP00000486804.1:n.*229T>C
NM_000431.3:c.782T>C	NP_000422.1:p.Val261Ala
NM_001114185.2:c.782T>C	NP_001107657.1:p.Val261Ala
NM_001301182.1:c.626T>C	NP_001288111.1:p.Val209Ala
XM_011538372.1:c.782T>C	XP_011536674.1:p.Val261Ala
XM_017019313.2:c.626T>C	XP_016874802.1:p.Val209Ala
XM_017019314.1:c.782T>C	XP_016874803.1:p.Val261Ala
XM_024448982.1:c.782T>C	XP_024304750.1:p.Val261Ala
NM_000431.4:c.782T>C MANE Select	NP_000422.1:p.Val261Ala
NM_001114185.3:c.782T>C	NP_001107657.1:p.Val261Ala
NM_001301182.2:c.626T>C	NP_001288111.1:p.Val209Ala