Canonical Allele Identifier: CA2062472506

Gene: MVK

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109594986T= , CM000674.2:g.109594986T=	GRCh38
NC_000012.11:g.110032791T= , CM000674.1:g.110032791T=	GRCh37
NC_000012.10:g.108517174T=	NCBI36
NG_007702.1:g.26292T= , LRG_156:g.26292T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539696.6:c.43-42T=	ENSP00000439134.1:n.43-42T=
ENST00000546277.6:c.886-42T=	ENSP00000438153.2:n.886-42T=
ENST00000636529.2:n.525-42T=
ENST00000697195.1:c.*650-42T=	ENSP00000513181.1:n.*650-42T=
ENST00000697196.1:c.*59-42T=	ENSP00000513182.1:n.*59-42T=
ENST00000697197.1:n.2915-42T=
ENST00000697198.1:n.1228T=
ENST00000228510.8:c.886-42T= MANE Select	ENSP00000228510.3:n.886-42T=
ENST00000636529.1:c.511-42T=
ENST00000636996.1:c.734-42T=
ENST00000228510.7:c.886-42T=	ENSP00000228510.3:n.886-42T=
ENST00000392727.7:c.730-42T=	ENSP00000376487.3:n.730-42T=
ENST00000447878.6:c.*333-42T=	ENSP00000415555.2:n.*333-42T=
ENST00000537237.5:c.*559-42T=	ENSP00000445382.1:n.*559-42T=
ENST00000539575.4:c.886-42T=	ENSP00000443551.2:n.886-42T=
ENST00000539696.5:c.43-42T=	ENSP00000439134.1:n.43-42T=
ENST00000540353.1:n.3119-42T=
ENST00000625889.2:c.730-42T=	ENSP00000486846.1:n.730-42T=
ENST00000629016.2:c.*333-42T=	ENSP00000486804.1:n.*333-42T=
NM_000431.3:c.886-42T=	NP_000422.1:n.886-42T=
NM_001114185.2:c.886-42T=	NP_001107657.1:n.886-42T=
NM_001301182.1:c.730-42T=	NP_001288111.1:n.730-42T=
XM_011538372.1:c.886-42T=	XP_011536674.1:n.886-42T=
XM_017019313.2:c.730-42T=	XP_016874802.1:n.730-42T=
XM_017019314.1:c.886-42T=	XP_016874803.1:n.886-42T=
NM_000431.4:c.886-42T= MANE Select	NP_000422.1:n.886-42T=
NM_001114185.3:c.886-42T=	NP_001107657.1:n.886-42T=
NM_001301182.2:c.730-42T=	NP_001288111.1:n.730-42T=