Canonical Allele Identifier: CA1562896464

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90778008C= , CM000667.2:g.90778008C=	GRCh38
NC_000005.9:g.90073825C= , CM000667.1:g.90073825C=	GRCh37
NC_000005.8:g.90109581C=	NCBI36
NG_007083.1:g.224209C=
NG_007083.2:g.253665C=

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.12631C= MANE Select	NP_115495.3:p.Arg4211=
ENST00000405460.9:c.12631C= MANE Select	ENSP00000384582.2:p.Arg4211=
NM_032119.3:c.12631C=	NP_115495.3:p.Arg4211=
NR_003149.1:n.12644C=
NR_003149.2:n.12647C=
ENST00000405460.6:c.12631C=	ENSP00000384582.2:p.Arg4211=
ENST00000425867.3:c.1585C=	ENSP00000392618.3:p.Arg529=
ENST00000639431.1:c.265+101799C=	ENSP00000491057.1:n.265+101799C=
ENST00000640464.1:n.3050C=
ENST00000640729.1:n.1208C=
XM_011543675.1:c.12628C=	XP_011541977.1:p.Arg4210=
XM_011543676.1:c.12550C=	XP_011541978.1:p.Arg4184=
XM_011543677.1:c.9934C=	XP_011541979.1:p.Arg3312=
XM_011543678.1:c.12631C=	XP_011541980.1:p.Arg4211=
XM_017009963.2:c.12652C=	XP_016865452.1:p.Arg4218=
XM_017009964.2:c.12649C=	XP_016865453.1:p.Arg4217=
XM_017009965.1:c.12649C=	XP_016865454.1:p.Arg4217=
XM_017009966.2:c.12571C=	XP_016865455.1:p.Arg4191=
XM_017009967.1:c.12556C=	XP_016865456.1:p.Arg4186=
XM_017009968.2:c.12652C=	XP_016865457.1:p.Arg4218=
XM_017009969.2:c.12652C=	XP_016865458.1:p.Arg4218=
XM_017009970.2:c.12652C=	XP_016865459.1:p.Arg4218=
XM_017009971.2:c.12652C=	XP_016865460.1:p.Arg4218=
XM_017009972.1:c.5770C=	XP_016865461.1:p.Arg1924=
XM_017009973.1:c.5749C=	XP_016865462.1:p.Arg1917=