Canonical Allele Identifier: CA1562859227

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692576T= , CM000667.2:g.90692576T=	GRCh38
NC_000005.9:g.89988393T= , CM000667.1:g.89988393T=	GRCh37
NC_000005.8:g.90024149T=	NCBI36
NG_007083.1:g.138777T=
NG_007083.2:g.168233T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.6952-29T= MANE Select	ENSP00000384582.2:n.6952-29T=
ENST00000639431.1:c.265+16367T=	ENSP00000491057.1:n.265+16367T=
ENST00000639473.1:n.2411-29T=
ENST00000640012.1:c.759-29T=
ENST00000640374.1:n.96-29T=
ENST00000640403.1:c.4243-29T=	ENSP00000492531.1:n.4243-29T=
ENST00000640779.1:c.1681-29T=
ENST00000405460.6:c.6952-29T=	ENSP00000384582.2:n.6952-29T=
NM_032119.3:c.6952-29T=	NP_115495.3:n.6952-29T=
NR_003149.1:n.6965-29T=
XM_011543675.1:c.6949-29T=	XP_011541977.1:n.6949-29T=
XM_011543676.1:c.6871-29T=	XP_011541978.1:n.6871-29T=
XM_011543677.1:c.4255-29T=	XP_011541979.1:n.4255-29T=
XM_011543678.1:c.6952-29T=	XP_011541980.1:n.6952-29T=
XM_011543679.1:c.6952-29T=	XP_011541981.1:n.6952-29T=
NM_032119.4:c.6952-29T= MANE Select	NP_115495.3:n.6952-29T=
XM_017009963.2:c.6952-29T=	XP_016865452.1:n.6952-29T=
XM_017009964.2:c.6949-29T=	XP_016865453.1:n.6949-29T=
XM_017009965.1:c.6949-29T=	XP_016865454.1:n.6949-29T=
XM_017009966.2:c.6871-29T=	XP_016865455.1:n.6871-29T=
XM_017009967.1:c.6856-29T=	XP_016865456.1:n.6856-29T=
XM_017009968.2:c.6952-29T=	XP_016865457.1:n.6952-29T=
XM_017009969.2:c.6952-29T=	XP_016865458.1:n.6952-29T=
XM_017009970.2:c.6952-29T=	XP_016865459.1:n.6952-29T=
XM_017009971.2:c.6952-29T=	XP_016865460.1:n.6952-29T=
XM_017009972.1:c.70-29T=	XP_016865461.1:n.70-29T=
XM_017009973.1:c.70-29T=	XP_016865462.1:n.70-29T=
XM_017009974.2:c.6952-29T=	XP_016865463.1:n.6952-29T=
NR_003149.2:n.6968-29T=