Canonical Allele Identifier: CA1562859743

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90693835T= , CM000667.2:g.90693835T=	GRCh38
NC_000005.9:g.89989652T= , CM000667.1:g.89989652T=	GRCh37
NC_000005.8:g.90025408T=	NCBI36
NG_007083.1:g.140036T=
NG_007083.2:g.169492T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.7134-55T= MANE Select	ENSP00000384582.2:n.7134-55T=
ENST00000639431.1:c.265+17626T=	ENSP00000491057.1:n.265+17626T=
ENST00000639473.1:n.2593-55T=
ENST00000640012.1:c.941-55T=
ENST00000640374.1:n.278-55T=
ENST00000640403.1:c.4425-55T=	ENSP00000492531.1:n.4425-55T=
ENST00000640779.1:c.1863-55T=
ENST00000405460.6:c.7134-55T=	ENSP00000384582.2:n.7134-55T=
NM_032119.3:c.7134-55T=	NP_115495.3:n.7134-55T=
NR_003149.1:n.7147-55T=
XM_011543675.1:c.7131-55T=	XP_011541977.1:n.7131-55T=
XM_011543676.1:c.7053-55T=	XP_011541978.1:n.7053-55T=
XM_011543677.1:c.4437-55T=	XP_011541979.1:n.4437-55T=
XM_011543678.1:c.7134-55T=	XP_011541980.1:n.7134-55T=
XM_011543679.1:c.7134-55T=	XP_011541981.1:n.7134-55T=
NM_032119.4:c.7134-55T= MANE Select	NP_115495.3:n.7134-55T=
XM_017009963.2:c.7134-55T=	XP_016865452.1:n.7134-55T=
XM_017009964.2:c.7131-55T=	XP_016865453.1:n.7131-55T=
XM_017009965.1:c.7131-55T=	XP_016865454.1:n.7131-55T=
XM_017009966.2:c.7053-55T=	XP_016865455.1:n.7053-55T=
XM_017009967.1:c.7038-55T=	XP_016865456.1:n.7038-55T=
XM_017009968.2:c.7134-55T=	XP_016865457.1:n.7134-55T=
XM_017009969.2:c.7134-55T=	XP_016865458.1:n.7134-55T=
XM_017009970.2:c.7134-55T=	XP_016865459.1:n.7134-55T=
XM_017009971.2:c.7134-55T=	XP_016865460.1:n.7134-55T=
XM_017009972.1:c.252-55T=	XP_016865461.1:n.252-55T=
XM_017009973.1:c.252-55T=	XP_016865462.1:n.252-55T=
XM_017009974.2:c.7134-55T=	XP_016865463.1:n.7134-55T=
NR_003149.2:n.7150-55T=