Canonical Allele Identifier: CA176195

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90681413G>A , CM000667.2:g.90681413G>A	GRCh38
NC_000005.9:g.89977230G>A , CM000667.1:g.89977230G>A	GRCh37
NC_000005.8:g.90012986G>A	NCBI36
NG_007083.1:g.127614G>A
NG_007083.2:g.157070G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.5623G>A MANE Select	NP_115495.3:p.Gly1875Arg
ENST00000405460.9:c.5623G>A MANE Select	ENSP00000384582.2:p.Gly1875Arg
NM_032119.3:c.5623G>A	NP_115495.3:p.Gly1875Arg
NR_003149.1:n.5719G>A
NR_003149.2:n.5722G>A
ENST00000405460.6:c.5623G>A	ENSP00000384582.2:p.Gly1875Arg
ENST00000639431.1:c.265+5204G>A	ENSP00000491057.1:n.265+5204G>A
ENST00000639473.1:n.1082G>A
ENST00000640012.1:c.123G>A
ENST00000640403.1:c.2914G>A	ENSP00000492531.1:p.Gly972Arg
ENST00000640779.1:c.435G>A
XM_011543675.1:c.5620G>A	XP_011541977.1:p.Gly1874Arg
XM_011543676.1:c.5542G>A	XP_011541978.1:p.Gly1848Arg
XM_011543677.1:c.2926G>A	XP_011541979.1:p.Gly976Arg
XM_011543678.1:c.5623G>A	XP_011541980.1:p.Gly1875Arg
XM_011543679.1:c.5623G>A	XP_011541981.1:p.Gly1875Arg
XM_017009963.2:c.5623G>A	XP_016865452.1:p.Gly1875Arg
XM_017009964.2:c.5620G>A	XP_016865453.1:p.Gly1874Arg
XM_017009965.1:c.5620G>A	XP_016865454.1:p.Gly1874Arg
XM_017009966.2:c.5542G>A	XP_016865455.1:p.Gly1848Arg
XM_017009967.1:c.5527G>A	XP_016865456.1:p.Gly1843Arg
XM_017009968.2:c.5623G>A	XP_016865457.1:p.Gly1875Arg
XM_017009969.2:c.5623G>A	XP_016865458.1:p.Gly1875Arg
XM_017009970.2:c.5623G>A	XP_016865459.1:p.Gly1875Arg
XM_017009971.2:c.5623G>A	XP_016865460.1:p.Gly1875Arg
XM_017009973.1:c.-1177G>A	XP_016865462.1:n.-1177G>A
XM_017009974.2:c.5623G>A	XP_016865463.1:p.Gly1875Arg