Canonical Allele Identifier: CA3340886

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90750636G>A , CM000667.2:g.90750636G>A	GRCh38
NC_000005.9:g.90046453G>A , CM000667.1:g.90046453G>A	GRCh37
NC_000005.8:g.90082209G>A	NCBI36
NG_007083.1:g.196837G>A
NG_007083.2:g.226293G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.11060G>A MANE Select	NP_115495.3:p.Arg3687His
ENST00000405460.9:c.11060G>A MANE Select	ENSP00000384582.2:p.Arg3687His
NM_032119.3:c.11060G>A	NP_115495.3:p.Arg3687His
NR_003149.1:n.11073G>A
NR_003149.2:n.11076G>A
ENST00000405460.6:c.11060G>A	ENSP00000384582.2:p.Arg3687His
ENST00000425867.3:c.191G>A	ENSP00000392618.3:p.Arg64His
ENST00000509621.1:c.3757G>A
ENST00000639431.1:c.265+74427G>A	ENSP00000491057.1:n.265+74427G>A
ENST00000640374.1:n.4204G>A
ENST00000640464.1:n.1479G>A
XM_011543675.1:c.11057G>A	XP_011541977.1:p.Arg3686His
XM_011543676.1:c.10979G>A	XP_011541978.1:p.Arg3660His
XM_011543677.1:c.8363G>A	XP_011541979.1:p.Arg2788His
XM_011543678.1:c.11060G>A	XP_011541980.1:p.Arg3687His
XM_017009963.2:c.11081G>A	XP_016865452.1:p.Arg3694His
XM_017009964.2:c.11078G>A	XP_016865453.1:p.Arg3693His
XM_017009965.1:c.11078G>A	XP_016865454.1:p.Arg3693His
XM_017009966.2:c.11000G>A	XP_016865455.1:p.Arg3667His
XM_017009967.1:c.10985G>A	XP_016865456.1:p.Arg3662His
XM_017009968.2:c.11081G>A	XP_016865457.1:p.Arg3694His
XM_017009969.2:c.11081G>A	XP_016865458.1:p.Arg3694His
XM_017009970.2:c.11081G>A	XP_016865459.1:p.Arg3694His
XM_017009971.2:c.11081G>A	XP_016865460.1:p.Arg3694His
XM_017009972.1:c.4199G>A	XP_016865461.1:p.Arg1400His
XM_017009973.1:c.4178G>A	XP_016865462.1:p.Arg1393His