Canonical Allele Identifier: CA386651312

Gene: MVK

Linked Data

• MyVariant Identifiers: chr12:g.110034279G>C (hg19) ; chr12:g.109596474G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109596474G>C , CM000674.2:g.109596474G>C	GRCh38
NC_000012.11:g.110034279G>C , CM000674.1:g.110034279G>C	GRCh37
NC_000012.10:g.108518662G>C	NCBI36
NG_007702.1:g.27780G>C , LRG_156:g.27780G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.245G>C	ENSP00000439134.1:p.Cys82Ser
ENST00000546277.6:c.1088G>C	ENSP00000438153.2:p.Cys363Ser
ENST00000636529.2:n.727G>C
ENST00000697195.1:c.*852G>C	ENSP00000513181.1:n.*852G>C
ENST00000697196.1:c.*261G>C	ENSP00000513182.1:n.*261G>C
ENST00000697197.1:n.3117G>C
ENST00000697198.1:n.1472G>C
ENST00000228510.8:c.1088G>C MANE Select	ENSP00000228510.3:p.Cys363Ser
ENST00000636529.1:c.713G>C
ENST00000636996.1:c.936G>C
ENST00000228510.7:c.1088G>C	ENSP00000228510.3:p.Cys363Ser
ENST00000392727.7:c.932G>C	ENSP00000376487.3:p.Cys311Ser
ENST00000447878.6:c.*535G>C	ENSP00000415555.2:n.*535G>C
ENST00000537237.5:c.*761G>C	ENSP00000445382.1:n.*761G>C
ENST00000539575.4:c.1088G>C	ENSP00000443551.2:p.Cys363Ser
ENST00000539696.5:c.245G>C	ENSP00000439134.1:p.Cys82Ser
ENST00000540353.1:n.3321G>C
ENST00000625889.2:c.932G>C	ENSP00000486846.1:p.Cys311Ser
ENST00000629016.2:c.*535G>C	ENSP00000486804.1:n.*535G>C
NM_000431.3:c.1088G>C	NP_000422.1:p.Cys363Ser
NM_001114185.2:c.1088G>C	NP_001107657.1:p.Cys363Ser
NM_001301182.1:c.932G>C	NP_001288111.1:p.Cys311Ser
XM_011538372.1:c.1088G>C	XP_011536674.1:p.Cys363Ser
XM_017019313.2:c.932G>C	XP_016874802.1:p.Cys311Ser
XM_017019314.1:c.1088G>C	XP_016874803.1:p.Cys363Ser
NM_000431.4:c.1088G>C MANE Select	NP_000422.1:p.Cys363Ser
NM_001114185.3:c.1088G>C	NP_001107657.1:p.Cys363Ser
NM_001301182.2:c.932G>C	NP_001288111.1:p.Cys311Ser