Canonical Allele Identifier: CA3339878

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90690887G>A , CM000667.2:g.90690887G>A	GRCh38
NC_000005.9:g.89986704G>A , CM000667.1:g.89986704G>A	GRCh37
NC_000005.8:g.90022460G>A	NCBI36
NG_007083.1:g.137088G>A
NG_007083.2:g.166544G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.6797G>A MANE Select	NP_115495.3:p.Gly2266Asp
ENST00000405460.9:c.6797G>A MANE Select	ENSP00000384582.2:p.Gly2266Asp
NM_032119.3:c.6797G>A	NP_115495.3:p.Gly2266Asp
NR_003149.1:n.6893G>A
NR_003149.2:n.6896G>A
ENST00000405460.6:c.6797G>A	ENSP00000384582.2:p.Gly2266Asp
ENST00000639431.1:c.265+14678G>A	ENSP00000491057.1:n.265+14678G>A
ENST00000639473.1:n.2256G>A
ENST00000640012.1:c.687G>A
ENST00000640403.1:c.4088G>A	ENSP00000492531.1:p.Gly1363Asp
ENST00000640779.1:c.1609G>A
XM_011543675.1:c.6794G>A	XP_011541977.1:p.Gly2265Asp
XM_011543676.1:c.6716G>A	XP_011541978.1:p.Gly2239Asp
XM_011543677.1:c.4100G>A	XP_011541979.1:p.Gly1367Asp
XM_011543678.1:c.6797G>A	XP_011541980.1:p.Gly2266Asp
XM_011543679.1:c.6797G>A	XP_011541981.1:p.Gly2266Asp
XM_017009963.2:c.6797G>A	XP_016865452.1:p.Gly2266Asp
XM_017009964.2:c.6794G>A	XP_016865453.1:p.Gly2265Asp
XM_017009965.1:c.6794G>A	XP_016865454.1:p.Gly2265Asp
XM_017009966.2:c.6716G>A	XP_016865455.1:p.Gly2239Asp
XM_017009967.1:c.6701G>A	XP_016865456.1:p.Gly2234Asp
XM_017009968.2:c.6797G>A	XP_016865457.1:p.Gly2266Asp
XM_017009969.2:c.6797G>A	XP_016865458.1:p.Gly2266Asp
XM_017009970.2:c.6797G>A	XP_016865459.1:p.Gly2266Asp
XM_017009971.2:c.6797G>A	XP_016865460.1:p.Gly2266Asp
XM_017009972.1:c.-3G>A	XP_016865461.1:n.-3G>A
XM_017009973.1:c.-3G>A	XP_016865462.1:n.-3G>A
XM_017009974.2:c.6797G>A	XP_016865463.1:p.Gly2266Asp