Canonical Allele Identifier: CA2062445014

Gene: MVK

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109591565A= , CM000674.2:g.109591565A=	GRCh38
NC_000012.11:g.110029370A= , CM000674.1:g.110029370A=	GRCh37
NC_000012.10:g.108513753A=	NCBI36
NG_007702.1:g.22871A= , LRG_156:g.22871A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.42+208A=	ENSP00000439134.1:n.42+208A=
ENST00000546277.6:c.885+208A=	ENSP00000438153.2:n.885+208A=
ENST00000636529.2:n.524+208A=
ENST00000697195.1:c.*649+208A=	ENSP00000513181.1:n.*649+208A=
ENST00000697196.1:c.*58+208A=	ENSP00000513182.1:n.*58+208A=
ENST00000697197.1:n.2914+208A=
ENST00000228510.8:c.885+208A= MANE Select	ENSP00000228510.3:n.885+208A=
ENST00000636529.1:c.510+208A=
ENST00000636996.1:c.733+208A=
ENST00000228510.7:c.885+208A=	ENSP00000228510.3:n.885+208A=
ENST00000392727.7:c.729+208A=	ENSP00000376487.3:n.729+208A=
ENST00000447878.6:c.*332+208A=	ENSP00000415555.2:n.*332+208A=
ENST00000537237.5:c.*558+208A=	ENSP00000445382.1:n.*558+208A=
ENST00000539575.4:c.885+208A=	ENSP00000443551.2:n.885+208A=
ENST00000539696.5:c.42+208A=	ENSP00000439134.1:n.42+208A=
ENST00000540353.1:n.3118+208A=
ENST00000625889.2:c.729+208A=	ENSP00000486846.1:n.729+208A=
ENST00000629016.2:c.*332+208A=	ENSP00000486804.1:n.*332+208A=
NM_000431.3:c.885+208A=	NP_000422.1:n.885+208A=
NM_001114185.2:c.885+208A=	NP_001107657.1:n.885+208A=
NM_001301182.1:c.729+208A=	NP_001288111.1:n.729+208A=
XM_011538372.1:c.885+208A=	XP_011536674.1:n.885+208A=
XM_017019313.2:c.729+208A=	XP_016874802.1:n.729+208A=
XM_017019314.1:c.885+208A=	XP_016874803.1:n.885+208A=
XM_024448982.1:c.1093A=	XP_024304750.1:p.Ser365=
NM_000431.4:c.885+208A= MANE Select	NP_000422.1:n.885+208A=
NM_001114185.3:c.885+208A=	NP_001107657.1:n.885+208A=
NM_001301182.2:c.729+208A=	NP_001288111.1:n.729+208A=