Canonical Allele Identifier: CA360372239

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90628687T>G , CM000667.2:g.90628687T>G	GRCh38
NC_000005.9:g.89924504T>G , CM000667.1:g.89924504T>G	GRCh37
NC_000005.8:g.89960260T>G	NCBI36
NG_007083.1:g.74888T>G
NG_007083.2:g.104344T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.1364T>G MANE Select	ENSP00000384582.2:p.Val455Gly
ENST00000504142.2:n.130T>G
ENST00000640083.1:n.1069T>G
ENST00000640109.1:n.1460T>G
ENST00000405460.6:c.1364T>G	ENSP00000384582.2:p.Val455Gly
ENST00000504142.1:c.129T>G
NM_032119.3:c.1364T>G	NP_115495.3:p.Val455Gly
NR_003149.1:n.1460T>G
XM_011543675.1:c.1364T>G	XP_011541977.1:p.Val455Gly
XM_011543676.1:c.1364T>G	XP_011541978.1:p.Val455Gly
XM_011543678.1:c.1364T>G	XP_011541980.1:p.Val455Gly
XM_011543679.1:c.1364T>G	XP_011541981.1:p.Val455Gly
NM_032119.4:c.1364T>G MANE Select	NP_115495.3:p.Val455Gly
XM_017009963.2:c.1364T>G	XP_016865452.1:p.Val455Gly
XM_017009964.2:c.1364T>G	XP_016865453.1:p.Val455Gly
XM_017009965.1:c.1361T>G	XP_016865454.1:p.Val454Gly
XM_017009966.2:c.1364T>G	XP_016865455.1:p.Val455Gly
XM_017009967.1:c.1268T>G	XP_016865456.1:p.Val423Gly
XM_017009968.2:c.1364T>G	XP_016865457.1:p.Val455Gly
XM_017009969.2:c.1364T>G	XP_016865458.1:p.Val455Gly
XM_017009970.2:c.1364T>G	XP_016865459.1:p.Val455Gly
XM_017009971.2:c.1364T>G	XP_016865460.1:p.Val455Gly
XM_017009974.2:c.1364T>G	XP_016865463.1:p.Val455Gly
NR_003149.2:n.1463T>G