Canonical Allele Identifier: CA6779377

Gene: MVK

Linked Data

• ClinVar Variation Id: 307099
• ClinVar RCV Id: RCV001711911 ; RCV002262959
• dbSNP Id: rs34975996
• ExAC: 12:110029057 C / A
• gnomAD v2: 12-110029057-C-A
• gnomAD v3: 12-109591252-C-A
• gnomAD v4: 12-109591252-C-A
• MyVariant Identifiers: chr12:g.110029057C>A (hg19) ; chr12:g.109591252C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109591252C>A , CM000674.2:g.109591252C>A	GRCh38
NC_000012.11:g.110029057C>A , CM000674.1:g.110029057C>A	GRCh37
NC_000012.10:g.108513440C>A	NCBI36
NG_007702.1:g.22558C>A , LRG_156:g.22558C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000539696.6:c.-64C>A	ENSP00000439134.1:n.-64C>A
ENST00000546277.6:c.780C>A	ENSP00000438153.2:p.Ile260=
ENST00000636529.2:n.419C>A
ENST00000697195.1:c.*544C>A	ENSP00000513181.1:n.*544C>A
ENST00000697196.1:c.868C>A	ENSP00000513182.1:p.Arg290Ser
ENST00000697197.1:n.2809C>A
ENST00000228510.8:c.780C>A MANE Select	ENSP00000228510.3:p.Ile260=
ENST00000636529.1:c.405C>A
ENST00000636996.1:c.628C>A
ENST00000228510.7:c.780C>A	ENSP00000228510.3:p.Ile260=
ENST00000392727.7:c.624C>A	ENSP00000376487.3:p.Ile208=
ENST00000447878.6:c.*227C>A	ENSP00000415555.2:n.*227C>A
ENST00000537237.5:c.*453C>A	ENSP00000445382.1:n.*453C>A
ENST00000539575.4:c.780C>A	ENSP00000443551.2:p.Ile260=
ENST00000539696.5:c.-64C>A	ENSP00000439134.1:n.-64C>A
ENST00000540353.1:n.3013C>A
ENST00000625889.2:c.624C>A	ENSP00000486846.1:p.Ile208=
ENST00000629016.2:c.*227C>A	ENSP00000486804.1:n.*227C>A
NM_000431.3:c.780C>A	NP_000422.1:p.Ile260=
NM_001114185.2:c.780C>A	NP_001107657.1:p.Ile260=
NM_001301182.1:c.624C>A	NP_001288111.1:p.Ile208=
XM_011538372.1:c.780C>A	XP_011536674.1:p.Ile260=
XM_017019313.2:c.624C>A	XP_016874802.1:p.Ile208=
XM_017019314.1:c.780C>A	XP_016874803.1:p.Ile260=
XM_024448982.1:c.780C>A	XP_024304750.1:p.Ile260=
NM_000431.4:c.780C>A MANE Select	NP_000422.1:p.Ile260=
NM_001114185.3:c.780C>A	NP_001107657.1:p.Ile260=
NM_001301182.2:c.624C>A	NP_001288111.1:p.Ile208=