Canonical Allele Identifier: CA360403449

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90657917T>G , CM000667.2:g.90657917T>G	GRCh38
NC_000005.9:g.89953734T>G , CM000667.1:g.89953734T>G	GRCh37
NC_000005.8:g.89989490T>G	NCBI36
NG_007083.1:g.104118T>G
NG_007083.2:g.133574T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.4391T>G MANE Select	NP_115495.3:p.Leu1464Arg
ENST00000405460.9:c.4391T>G MANE Select	ENSP00000384582.2:p.Leu1464Arg
NM_032119.3:c.4391T>G	NP_115495.3:p.Leu1464Arg
NR_003149.1:n.4487T>G
NR_003149.2:n.4490T>G
ENST00000405460.6:c.4391T>G	ENSP00000384582.2:p.Leu1464Arg
ENST00000639676.1:n.1989T>G
ENST00000640403.1:c.1682T>G	ENSP00000492531.1:p.Leu561Arg
XM_011543675.1:c.4391T>G	XP_011541977.1:p.Leu1464Arg
XM_011543676.1:c.4391T>G	XP_011541978.1:p.Leu1464Arg
XM_011543677.1:c.1694T>G	XP_011541979.1:p.Leu565Arg
XM_011543678.1:c.4391T>G	XP_011541980.1:p.Leu1464Arg
XM_011543679.1:c.4391T>G	XP_011541981.1:p.Leu1464Arg
XM_017009963.2:c.4391T>G	XP_016865452.1:p.Leu1464Arg
XM_017009964.2:c.4391T>G	XP_016865453.1:p.Leu1464Arg
XM_017009965.1:c.4388T>G	XP_016865454.1:p.Leu1463Arg
XM_017009966.2:c.4391T>G	XP_016865455.1:p.Leu1464Arg
XM_017009967.1:c.4295T>G	XP_016865456.1:p.Leu1432Arg
XM_017009968.2:c.4391T>G	XP_016865457.1:p.Leu1464Arg
XM_017009969.2:c.4391T>G	XP_016865458.1:p.Leu1464Arg
XM_017009970.2:c.4391T>G	XP_016865459.1:p.Leu1464Arg
XM_017009971.2:c.4391T>G	XP_016865460.1:p.Leu1464Arg
XM_017009974.2:c.4391T>G	XP_016865463.1:p.Leu1464Arg