Canonical Allele Identifier: CA6779456

Gene: MVK

Linked Data

• ClinVar Variation Id: 1139653
• ClinVar RCV Id: RCV001476430
• dbSNP Id: rs368066027
• ExAC: 12:110034307 C / T
• gnomAD v2: 12-110034307-C-T
• gnomAD v3: 12-109596502-C-T
• gnomAD v4: 12-109596502-C-T
• MyVariant Identifiers: chr12:g.110034307C>T (hg19) ; chr12:g.109596502C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109596502C>T , CM000674.2:g.109596502C>T	GRCh38
NC_000012.11:g.110034307C>T , CM000674.1:g.110034307C>T	GRCh37
NC_000012.10:g.108518690C>T	NCBI36
NG_007702.1:g.27808C>T , LRG_156:g.27808C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.273C>T	ENSP00000439134.1:p.Ile91=
ENST00000546277.6:c.1116C>T	ENSP00000438153.2:p.Ile372=
ENST00000636529.2:n.755C>T
ENST00000697195.1:c.*880C>T	ENSP00000513181.1:n.*880C>T
ENST00000697196.1:c.*289C>T	ENSP00000513182.1:n.*289C>T
ENST00000697197.1:n.3145C>T
ENST00000697198.1:n.1500C>T
ENST00000228510.8:c.1116C>T MANE Select	ENSP00000228510.3:p.Ile372=
ENST00000636529.1:c.741C>T
ENST00000636996.1:c.964C>T
ENST00000228510.7:c.1116C>T	ENSP00000228510.3:p.Ile372=
ENST00000392727.7:c.960C>T	ENSP00000376487.3:p.Ile320=
ENST00000447878.6:c.*563C>T	ENSP00000415555.2:n.*563C>T
ENST00000537237.5:c.*789C>T	ENSP00000445382.1:n.*789C>T
ENST00000539575.4:c.1116C>T	ENSP00000443551.2:p.Ile372=
ENST00000539696.5:c.273C>T	ENSP00000439134.1:p.Ile91=
ENST00000540353.1:n.3349C>T
ENST00000625889.2:c.960C>T	ENSP00000486846.1:p.Ile320=
ENST00000629016.2:c.*563C>T	ENSP00000486804.1:n.*563C>T
NM_000431.3:c.1116C>T	NP_000422.1:p.Ile372=
NM_001114185.2:c.1116C>T	NP_001107657.1:p.Ile372=
NM_001301182.1:c.960C>T	NP_001288111.1:p.Ile320=
XM_011538372.1:c.1116C>T	XP_011536674.1:p.Ile372=
XM_017019313.2:c.960C>T	XP_016874802.1:p.Ile320=
XM_017019314.1:c.1116C>T	XP_016874803.1:p.Ile372=
NM_000431.4:c.1116C>T MANE Select	NP_000422.1:p.Ile372=
NM_001114185.3:c.1116C>T	NP_001107657.1:p.Ile372=
NM_001301182.2:c.960C>T	NP_001288111.1:p.Ile320=