Canonical Allele Identifier: CA386650825

Gene: MVK

Linked Data

• MyVariant Identifiers: chr12:g.110032936A>C (hg19) ; chr12:g.109595131A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109595131A>C , CM000674.2:g.109595131A>C	GRCh38
NC_000012.11:g.110032936A>C , CM000674.1:g.110032936A>C	GRCh37
NC_000012.10:g.108517319A>C	NCBI36
NG_007702.1:g.26437A>C , LRG_156:g.26437A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000539696.6:c.146A>C	ENSP00000439134.1:p.Lys49Thr
ENST00000546277.6:c.989A>C	ENSP00000438153.2:p.Lys330Thr
ENST00000636529.2:n.628A>C
ENST00000697195.1:c.*753A>C	ENSP00000513181.1:n.*753A>C
ENST00000697196.1:c.*162A>C	ENSP00000513182.1:n.*162A>C
ENST00000697197.1:n.3018A>C
ENST00000697198.1:n.1373A>C
ENST00000228510.8:c.989A>C MANE Select	ENSP00000228510.3:p.Lys330Thr
ENST00000636529.1:c.614A>C
ENST00000636996.1:c.837A>C
ENST00000228510.7:c.989A>C	ENSP00000228510.3:p.Lys330Thr
ENST00000392727.7:c.833A>C	ENSP00000376487.3:p.Lys278Thr
ENST00000447878.6:c.*436A>C	ENSP00000415555.2:n.*436A>C
ENST00000537237.5:c.*662A>C	ENSP00000445382.1:n.*662A>C
ENST00000539575.4:c.989A>C	ENSP00000443551.2:p.Lys330Thr
ENST00000539696.5:c.146A>C	ENSP00000439134.1:p.Lys49Thr
ENST00000540353.1:n.3222A>C
ENST00000625889.2:c.833A>C	ENSP00000486846.1:p.Lys278Thr
ENST00000629016.2:c.*436A>C	ENSP00000486804.1:n.*436A>C
NM_000431.3:c.989A>C	NP_000422.1:p.Lys330Thr
NM_001114185.2:c.989A>C	NP_001107657.1:p.Lys330Thr
NM_001301182.1:c.833A>C	NP_001288111.1:p.Lys278Thr
XM_011538372.1:c.989A>C	XP_011536674.1:p.Lys330Thr
XM_017019313.2:c.833A>C	XP_016874802.1:p.Lys278Thr
XM_017019314.1:c.989A>C	XP_016874803.1:p.Lys330Thr
NM_000431.4:c.989A>C MANE Select	NP_000422.1:p.Lys330Thr
NM_001114185.3:c.989A>C	NP_001107657.1:p.Lys330Thr
NM_001301182.2:c.833A>C	NP_001288111.1:p.Lys278Thr