Canonical Allele Identifier: CA3340226

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90704394G>A , CM000667.2:g.90704394G>A	GRCh38
NC_000005.9:g.90000211G>A , CM000667.1:g.90000211G>A	GRCh37
NC_000005.8:g.90035967G>A	NCBI36
NG_007083.1:g.150595G>A
NG_007083.2:g.180051G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.8292G>A MANE Select	NP_115495.3:p.Ser2764=
ENST00000405460.9:c.8292G>A MANE Select	ENSP00000384582.2:p.Ser2764=
NM_032119.3:c.8292G>A	NP_115495.3:p.Ser2764=
NR_003149.1:n.8305G>A
NR_003149.2:n.8308G>A
ENST00000405460.6:c.8292G>A	ENSP00000384582.2:p.Ser2764=
ENST00000509621.1:c.989G>A
ENST00000639431.1:c.265+28185G>A	ENSP00000491057.1:n.265+28185G>A
ENST00000639473.1:n.3751G>A
ENST00000640012.1:c.2099G>A
ENST00000640374.1:n.1436G>A
ENST00000640403.1:c.5583G>A	ENSP00000492531.1:p.Ser1861=
ENST00000640779.1:c.3021G>A
XM_011543675.1:c.8289G>A	XP_011541977.1:p.Ser2763=
XM_011543676.1:c.8211G>A	XP_011541978.1:p.Ser2737=
XM_011543677.1:c.5595G>A	XP_011541979.1:p.Ser1865=
XM_011543678.1:c.8292G>A	XP_011541980.1:p.Ser2764=
XM_011543679.1:c.8292G>A	XP_011541981.1:p.Ser2764=
XM_017009963.2:c.8292G>A	XP_016865452.1:p.Ser2764=
XM_017009964.2:c.8289G>A	XP_016865453.1:p.Ser2763=
XM_017009965.1:c.8289G>A	XP_016865454.1:p.Ser2763=
XM_017009966.2:c.8211G>A	XP_016865455.1:p.Ser2737=
XM_017009967.1:c.8196G>A	XP_016865456.1:p.Ser2732=
XM_017009968.2:c.8292G>A	XP_016865457.1:p.Ser2764=
XM_017009969.2:c.8292G>A	XP_016865458.1:p.Ser2764=
XM_017009970.2:c.8292G>A	XP_016865459.1:p.Ser2764=
XM_017009971.2:c.8292G>A	XP_016865460.1:p.Ser2764=
XM_017009972.1:c.1410G>A	XP_016865461.1:p.Ser470=
XM_017009973.1:c.1410G>A	XP_016865462.1:p.Ser470=
XM_017009974.2:c.8292G>A	XP_016865463.1:p.Ser2764=