Canonical Allele Identifier: CA3339385

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90658207G>A , CM000667.2:g.90658207G>A	GRCh38
NC_000005.9:g.89954024G>A , CM000667.1:g.89954024G>A	GRCh37
NC_000005.8:g.89989780G>A	NCBI36
NG_007083.1:g.104408G>A
NG_007083.2:g.133864G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.4681G>A MANE Select	NP_115495.3:p.Ala1561Thr
ENST00000405460.9:c.4681G>A MANE Select	ENSP00000384582.2:p.Ala1561Thr
NM_032119.3:c.4681G>A	NP_115495.3:p.Ala1561Thr
NR_003149.1:n.4777G>A
NR_003149.2:n.4780G>A
ENST00000405460.6:c.4681G>A	ENSP00000384582.2:p.Ala1561Thr
ENST00000639473.1:n.140G>A
ENST00000639676.1:n.2279G>A
ENST00000640403.1:c.1972G>A	ENSP00000492531.1:p.Ala658Thr
XM_011543675.1:c.4681G>A	XP_011541977.1:p.Ala1561Thr
XM_011543676.1:c.4681G>A	XP_011541978.1:p.Ala1561Thr
XM_011543677.1:c.1984G>A	XP_011541979.1:p.Ala662Thr
XM_011543678.1:c.4681G>A	XP_011541980.1:p.Ala1561Thr
XM_011543679.1:c.4681G>A	XP_011541981.1:p.Ala1561Thr
XM_017009963.2:c.4681G>A	XP_016865452.1:p.Ala1561Thr
XM_017009964.2:c.4681G>A	XP_016865453.1:p.Ala1561Thr
XM_017009965.1:c.4678G>A	XP_016865454.1:p.Ala1560Thr
XM_017009966.2:c.4681G>A	XP_016865455.1:p.Ala1561Thr
XM_017009967.1:c.4585G>A	XP_016865456.1:p.Ala1529Thr
XM_017009968.2:c.4681G>A	XP_016865457.1:p.Ala1561Thr
XM_017009969.2:c.4681G>A	XP_016865458.1:p.Ala1561Thr
XM_017009970.2:c.4681G>A	XP_016865459.1:p.Ala1561Thr
XM_017009971.2:c.4681G>A	XP_016865460.1:p.Ala1561Thr
XM_017009974.2:c.4681G>A	XP_016865463.1:p.Ala1561Thr