Canonical Allele Identifier: CA2062473152

Gene: MVK

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109596599C= , CM000674.2:g.109596599C=	GRCh38
NC_000012.11:g.110034404C= , CM000674.1:g.110034404C=	GRCh37
NC_000012.10:g.108518787C=	NCBI36
NG_007702.1:g.27905C= , LRG_156:g.27905C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.*22C=	ENSP00000439134.1:n.*22C=
ENST00000546277.6:c.*22C=	ENSP00000438153.2:n.*22C=
ENST00000636529.2:n.852C=
ENST00000697195.1:c.*977C=	ENSP00000513181.1:n.*977C=
ENST00000697196.1:c.*386C=	ENSP00000513182.1:n.*386C=
ENST00000697197.1:n.3242C=
ENST00000697198.1:n.1597C=
ENST00000228510.8:c.*22C= MANE Select	ENSP00000228510.3:n.*22C=
ENST00000636529.1:c.838C=
ENST00000636996.1:c.1061C=
ENST00000228510.7:c.*22C=	ENSP00000228510.3:n.*22C=
ENST00000392727.7:c.*22C=	ENSP00000376487.3:n.*22C=
ENST00000447878.6:c.*660C=	ENSP00000415555.2:n.*660C=
ENST00000539575.4:c.*22C=	ENSP00000443551.2:n.*22C=
ENST00000539696.5:c.*22C=	ENSP00000439134.1:n.*22C=
ENST00000540353.1:n.3446C=
ENST00000625889.2:c.*22C=	ENSP00000486846.1:n.*22C=
ENST00000629016.2:c.*660C=	ENSP00000486804.1:n.*660C=
NM_000431.3:c.*22C=	NP_000422.1:n.*22C=
NM_001114185.2:c.*22C=	NP_001107657.1:n.*22C=
NM_001301182.1:c.*22C=	NP_001288111.1:n.*22C=
XM_011538372.1:c.*22C=	XP_011536674.1:n.*22C=
XM_017019313.2:c.*22C=	XP_016874802.1:n.*22C=
XM_017019314.1:c.*22C=	XP_016874803.1:n.*22C=
NM_000431.4:c.*22C= MANE Select	NP_000422.1:n.*22C=
NM_001114185.3:c.*22C=	NP_001107657.1:n.*22C=
NM_001301182.2:c.*22C=	NP_001288111.1:n.*22C=