Canonical Allele Identifier: CA481714930

Gene: MVK

Linked Data

• dbSNP Id: rs376025633
• gnomAD v4: 12-109591342-G-A
• MyVariant Identifiers: chr12:g.110029147G>A (hg19) ; chr12:g.109591342G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109591342G>A , CM000674.2:g.109591342G>A	GRCh38
NC_000012.11:g.110029147G>A , CM000674.1:g.110029147G>A	GRCh37
NC_000012.10:g.108513530G>A	NCBI36
NG_007702.1:g.22648G>A , LRG_156:g.22648G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.27G>A	ENSP00000439134.1:p.Gln9=
ENST00000546277.6:c.870G>A	ENSP00000438153.2:p.Gln290=
ENST00000636529.2:n.509G>A
ENST00000697195.1:c.*634G>A	ENSP00000513181.1:n.*634G>A
ENST00000697196.1:c.*43G>A	ENSP00000513182.1:n.*43G>A
ENST00000697197.1:n.2899G>A
ENST00000228510.8:c.870G>A MANE Select	ENSP00000228510.3:p.Gln290=
ENST00000636529.1:c.495G>A
ENST00000636996.1:c.718G>A
ENST00000228510.7:c.870G>A	ENSP00000228510.3:p.Gln290=
ENST00000392727.7:c.714G>A	ENSP00000376487.3:p.Gln238=
ENST00000447878.6:c.*317G>A	ENSP00000415555.2:n.*317G>A
ENST00000537237.5:c.*543G>A	ENSP00000445382.1:n.*543G>A
ENST00000539575.4:c.870G>A	ENSP00000443551.2:p.Gln290=
ENST00000539696.5:c.27G>A	ENSP00000439134.1:p.Gln9=
ENST00000540353.1:n.3103G>A
ENST00000625889.2:c.714G>A	ENSP00000486846.1:p.Gln238=
ENST00000629016.2:c.*317G>A	ENSP00000486804.1:n.*317G>A
NM_000431.3:c.870G>A	NP_000422.1:p.Gln290=
NM_001114185.2:c.870G>A	NP_001107657.1:p.Gln290=
NM_001301182.1:c.714G>A	NP_001288111.1:p.Gln238=
XM_011538372.1:c.870G>A	XP_011536674.1:p.Gln290=
XM_017019313.2:c.714G>A	XP_016874802.1:p.Gln238=
XM_017019314.1:c.870G>A	XP_016874803.1:p.Gln290=
XM_024448982.1:c.870G>A	XP_024304750.1:p.Gln290=
NM_000431.4:c.870G>A MANE Select	NP_000422.1:p.Gln290=
NM_001114185.3:c.870G>A	NP_001107657.1:p.Gln290=
NM_001301182.2:c.714G>A	NP_001288111.1:p.Gln238=