Canonical Allele Identifier: CA1562829331

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90627338A= , CM000667.2:g.90627338A=	GRCh38
NC_000005.9:g.89923155A= , CM000667.1:g.89923155A=	GRCh37
NC_000005.8:g.89958911A=	NCBI36
NG_007083.1:g.73539A=
NG_007083.2:g.102995A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.800A= MANE Select	ENSP00000384582.2:p.Gln267=
ENST00000640083.1:n.505A=
ENST00000640109.1:n.896A=
ENST00000640281.1:n.859A=
ENST00000405460.6:c.800A=	ENSP00000384582.2:p.Gln267=
NM_032119.3:c.800A=	NP_115495.3:p.Gln267=
NR_003149.1:n.896A=
XM_011543675.1:c.800A=	XP_011541977.1:p.Gln267=
XM_011543676.1:c.800A=	XP_011541978.1:p.Gln267=
XM_011543678.1:c.800A=	XP_011541980.1:p.Gln267=
XM_011543679.1:c.800A=	XP_011541981.1:p.Gln267=
NM_032119.4:c.800A= MANE Select	NP_115495.3:p.Gln267=
XM_017009963.2:c.800A=	XP_016865452.1:p.Gln267=
XM_017009964.2:c.800A=	XP_016865453.1:p.Gln267=
XM_017009965.1:c.797A=	XP_016865454.1:p.Gln266=
XM_017009966.2:c.800A=	XP_016865455.1:p.Gln267=
XM_017009967.1:c.704A=	XP_016865456.1:p.Gln235=
XM_017009968.2:c.800A=	XP_016865457.1:p.Gln267=
XM_017009969.2:c.800A=	XP_016865458.1:p.Gln267=
XM_017009970.2:c.800A=	XP_016865459.1:p.Gln267=
XM_017009971.2:c.800A=	XP_016865460.1:p.Gln267=
XM_017009974.2:c.800A=	XP_016865463.1:p.Gln267=
NR_003149.2:n.899A=