Canonical Allele Identifier: CA386649191

Gene: MVK

Linked Data

• MyVariant Identifiers: chr12:g.110029049C>G (hg19) ; chr12:g.109591244C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109591244C>G , CM000674.2:g.109591244C>G	GRCh38
NC_000012.11:g.110029049C>G , CM000674.1:g.110029049C>G	GRCh37
NC_000012.10:g.108513432C>G	NCBI36
NG_007702.1:g.22550C>G , LRG_156:g.22550C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.-72C>G	ENSP00000439134.1:n.-72C>G
ENST00000546277.6:c.772C>G	ENSP00000438153.2:p.Pro258Ala
ENST00000636529.2:n.411C>G
ENST00000697195.1:c.*536C>G	ENSP00000513181.1:n.*536C>G
ENST00000697196.1:c.860C>G	ENSP00000513182.1:p.Pro287Arg
ENST00000697197.1:n.2801C>G
ENST00000228510.8:c.772C>G MANE Select	ENSP00000228510.3:p.Pro258Ala
ENST00000636529.1:c.397C>G
ENST00000636996.1:c.620C>G
ENST00000228510.7:c.772C>G	ENSP00000228510.3:p.Pro258Ala
ENST00000392727.7:c.616C>G	ENSP00000376487.3:p.Pro206Ala
ENST00000447878.6:c.*219C>G	ENSP00000415555.2:n.*219C>G
ENST00000537237.5:c.*445C>G	ENSP00000445382.1:n.*445C>G
ENST00000539575.4:c.772C>G	ENSP00000443551.2:p.Pro258Ala
ENST00000539696.5:c.-72C>G	ENSP00000439134.1:n.-72C>G
ENST00000540353.1:n.3005C>G
ENST00000625889.2:c.616C>G	ENSP00000486846.1:p.Pro206Ala
ENST00000629016.2:c.*219C>G	ENSP00000486804.1:n.*219C>G
NM_000431.3:c.772C>G	NP_000422.1:p.Pro258Ala
NM_001114185.2:c.772C>G	NP_001107657.1:p.Pro258Ala
NM_001301182.1:c.616C>G	NP_001288111.1:p.Pro206Ala
XM_011538372.1:c.772C>G	XP_011536674.1:p.Pro258Ala
XM_017019313.2:c.616C>G	XP_016874802.1:p.Pro206Ala
XM_017019314.1:c.772C>G	XP_016874803.1:p.Pro258Ala
XM_024448982.1:c.772C>G	XP_024304750.1:p.Pro258Ala
NM_000431.4:c.772C>G MANE Select	NP_000422.1:p.Pro258Ala
NM_001114185.3:c.772C>G	NP_001107657.1:p.Pro258Ala
NM_001301182.2:c.616C>G	NP_001288111.1:p.Pro206Ala