Canonical Allele Identifier: CA2241206753

Gene: MVD

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88655134G= , CM000678.2:g.88655134G=	GRCh38
NC_000016.9:g.88721542G= , CM000678.1:g.88721542G=	GRCh37
NC_000016.8:g.87249043G=	NCBI36
NG_007291.1:g.916C= , LRG_52:g.916C=
NG_052674.1:g.13020C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000301012.8:c.897+65C= MANE Select	ENSP00000301012.3:n.897+65C=
ENST00000301012.7:c.897+65C=	ENSP00000301012.3:n.897+65C=
ENST00000565149.5:n.1456+65C=
ENST00000620002.4:c.380+65C=	ENSP00000479264.1:n.380+65C=
NM_002461.2:c.897+65C=	NP_002452.1:n.897+65C=
XM_011523086.1:c.999+65C=	XP_011521388.1:n.999+65C=
XM_011523087.1:c.936+65C=	XP_011521389.1:n.936+65C=
XM_011523088.1:c.834+65C=	XP_011521390.1:n.834+65C=
XM_011523089.1:c.546+65C=	XP_011521391.1:n.546+65C=
XM_011523086.2:c.999+65C=	XP_011521388.1:n.999+65C=
XM_011523087.2:c.936+65C=	XP_011521389.1:n.936+65C=
XM_011523088.2:c.834+65C=	XP_011521390.1:n.834+65C=
XM_011523089.2:c.546+65C=	XP_011521391.1:n.546+65C=
NM_002461.3:c.897+65C= MANE Select	NP_002452.1:n.897+65C=