Canonical Allele Identifier: CA2241206756

Gene: MVD

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88655137A= , CM000678.2:g.88655137A=	GRCh38
NC_000016.9:g.88721545A= , CM000678.1:g.88721545A=	GRCh37
NC_000016.8:g.87249046A=	NCBI36
NG_007291.1:g.913T= , LRG_52:g.913T=
NG_052674.1:g.13017T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000301012.8:c.897+62T= MANE Select	ENSP00000301012.3:n.897+62T=
ENST00000301012.7:c.897+62T=	ENSP00000301012.3:n.897+62T=
ENST00000565149.5:n.1456+62T=
ENST00000620002.4:c.380+62T=	ENSP00000479264.1:n.380+62T=
NM_002461.2:c.897+62T=	NP_002452.1:n.897+62T=
XM_011523086.1:c.999+62T=	XP_011521388.1:n.999+62T=
XM_011523087.1:c.936+62T=	XP_011521389.1:n.936+62T=
XM_011523088.1:c.834+62T=	XP_011521390.1:n.834+62T=
XM_011523089.1:c.546+62T=	XP_011521391.1:n.546+62T=
XM_011523086.2:c.999+62T=	XP_011521388.1:n.999+62T=
XM_011523087.2:c.936+62T=	XP_011521389.1:n.936+62T=
XM_011523088.2:c.834+62T=	XP_011521390.1:n.834+62T=
XM_011523089.2:c.546+62T=	XP_011521391.1:n.546+62T=
NM_002461.3:c.897+62T= MANE Select	NP_002452.1:n.897+62T=