Canonical Allele Identifier: CA149928

Gene: MVK

Linked Data

• ClinVar Variation Id: 97637
• ClinVar RCV Id: RCV000083889 ; RCV001701744
• dbSNP Id: rs104895305
• ExAC: 12:110032872 G / A
• gnomAD v2: 12-110032872-G-A
• gnomAD v4: 12-109595067-G-A
• MyVariant Identifiers: chr12:g.110032872G>A (hg19) ; chr12:g.109595067G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109595067G>A , CM000674.2:g.109595067G>A	GRCh38
NC_000012.11:g.110032872G>A , CM000674.1:g.110032872G>A	GRCh37
NC_000012.10:g.108517255G>A	NCBI36
NG_007702.1:g.26373G>A , LRG_156:g.26373G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000539696.6:c.82G>A	ENSP00000439134.1:p.Gly28Ser
ENST00000546277.6:c.925G>A	ENSP00000438153.2:p.Gly309Ser
ENST00000636529.2:n.564G>A
ENST00000697195.1:c.*689G>A	ENSP00000513181.1:n.*689G>A
ENST00000697196.1:c.*98G>A	ENSP00000513182.1:n.*98G>A
ENST00000697197.1:n.2954G>A
ENST00000697198.1:n.1309G>A
ENST00000228510.8:c.925G>A MANE Select	ENSP00000228510.3:p.Gly309Ser
ENST00000636529.1:c.550G>A
ENST00000636996.1:c.773G>A
ENST00000228510.7:c.925G>A	ENSP00000228510.3:p.Gly309Ser
ENST00000392727.7:c.769G>A	ENSP00000376487.3:p.Gly257Ser
ENST00000447878.6:c.*372G>A	ENSP00000415555.2:n.*372G>A
ENST00000537237.5:c.*598G>A	ENSP00000445382.1:n.*598G>A
ENST00000539575.4:c.925G>A	ENSP00000443551.2:p.Gly309Ser
ENST00000539696.5:c.82G>A	ENSP00000439134.1:p.Gly28Ser
ENST00000540353.1:n.3158G>A
ENST00000625889.2:c.769G>A	ENSP00000486846.1:p.Gly257Ser
ENST00000629016.2:c.*372G>A	ENSP00000486804.1:n.*372G>A
NM_000431.3:c.925G>A	NP_000422.1:p.Gly309Ser
NM_001114185.2:c.925G>A	NP_001107657.1:p.Gly309Ser
NM_001301182.1:c.769G>A	NP_001288111.1:p.Gly257Ser
XM_011538372.1:c.925G>A	XP_011536674.1:p.Gly309Ser
XM_017019313.2:c.769G>A	XP_016874802.1:p.Gly257Ser
XM_017019314.1:c.925G>A	XP_016874803.1:p.Gly309Ser
NM_000431.4:c.925G>A MANE Select	NP_000422.1:p.Gly309Ser
NM_001114185.3:c.925G>A	NP_001107657.1:p.Gly309Ser
NM_001301182.2:c.769G>A	NP_001288111.1:p.Gly257Ser