Canonical Allele Identifier: CA386650732

Gene: MVK

Linked Data

• MyVariant Identifiers: chr12:g.110032916G>T (hg19) ; chr12:g.109595111G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109595111G>T , CM000674.2:g.109595111G>T	GRCh38
NC_000012.11:g.110032916G>T , CM000674.1:g.110032916G>T	GRCh37
NC_000012.10:g.108517299G>T	NCBI36
NG_007702.1:g.26417G>T , LRG_156:g.26417G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.126G>T	ENSP00000439134.1:p.Arg42Ser
ENST00000546277.6:c.969G>T	ENSP00000438153.2:p.Arg323Ser
ENST00000636529.2:n.608G>T
ENST00000697195.1:c.*733G>T	ENSP00000513181.1:n.*733G>T
ENST00000697196.1:c.*142G>T	ENSP00000513182.1:n.*142G>T
ENST00000697197.1:n.2998G>T
ENST00000697198.1:n.1353G>T
ENST00000228510.8:c.969G>T MANE Select	ENSP00000228510.3:p.Arg323Ser
ENST00000636529.1:c.594G>T
ENST00000636996.1:c.817G>T
ENST00000228510.7:c.969G>T	ENSP00000228510.3:p.Arg323Ser
ENST00000392727.7:c.813G>T	ENSP00000376487.3:p.Arg271Ser
ENST00000447878.6:c.*416G>T	ENSP00000415555.2:n.*416G>T
ENST00000537237.5:c.*642G>T	ENSP00000445382.1:n.*642G>T
ENST00000539575.4:c.969G>T	ENSP00000443551.2:p.Arg323Ser
ENST00000539696.5:c.126G>T	ENSP00000439134.1:p.Arg42Ser
ENST00000540353.1:n.3202G>T
ENST00000625889.2:c.813G>T	ENSP00000486846.1:p.Arg271Ser
ENST00000629016.2:c.*416G>T	ENSP00000486804.1:n.*416G>T
NM_000431.3:c.969G>T	NP_000422.1:p.Arg323Ser
NM_001114185.2:c.969G>T	NP_001107657.1:p.Arg323Ser
NM_001301182.1:c.813G>T	NP_001288111.1:p.Arg271Ser
XM_011538372.1:c.969G>T	XP_011536674.1:p.Arg323Ser
XM_017019313.2:c.813G>T	XP_016874802.1:p.Arg271Ser
XM_017019314.1:c.969G>T	XP_016874803.1:p.Arg323Ser
NM_000431.4:c.969G>T MANE Select	NP_000422.1:p.Arg323Ser
NM_001114185.3:c.969G>T	NP_001107657.1:p.Arg323Ser
NM_001301182.2:c.813G>T	NP_001288111.1:p.Arg271Ser