Canonical Allele Identifier: CA3339628

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90681447C>G , CM000667.2:g.90681447C>G	GRCh38
NC_000005.9:g.89977264C>G , CM000667.1:g.89977264C>G	GRCh37
NC_000005.8:g.90013020C>G	NCBI36
NG_007083.1:g.127648C>G
NG_007083.2:g.157104C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.5657C>G MANE Select	NP_115495.3:p.Thr1886Arg
ENST00000405460.9:c.5657C>G MANE Select	ENSP00000384582.2:p.Thr1886Arg
NM_032119.3:c.5657C>G	NP_115495.3:p.Thr1886Arg
NR_003149.1:n.5753C>G
NR_003149.2:n.5756C>G
ENST00000405460.6:c.5657C>G	ENSP00000384582.2:p.Thr1886Arg
ENST00000639431.1:c.265+5238C>G	ENSP00000491057.1:n.265+5238C>G
ENST00000639473.1:n.1116C>G
ENST00000640012.1:c.157C>G
ENST00000640403.1:c.2948C>G	ENSP00000492531.1:p.Thr983Arg
ENST00000640779.1:c.469C>G
XM_011543675.1:c.5654C>G	XP_011541977.1:p.Thr1885Arg
XM_011543676.1:c.5576C>G	XP_011541978.1:p.Thr1859Arg
XM_011543677.1:c.2960C>G	XP_011541979.1:p.Thr987Arg
XM_011543678.1:c.5657C>G	XP_011541980.1:p.Thr1886Arg
XM_011543679.1:c.5657C>G	XP_011541981.1:p.Thr1886Arg
XM_017009963.2:c.5657C>G	XP_016865452.1:p.Thr1886Arg
XM_017009964.2:c.5654C>G	XP_016865453.1:p.Thr1885Arg
XM_017009965.1:c.5654C>G	XP_016865454.1:p.Thr1885Arg
XM_017009966.2:c.5576C>G	XP_016865455.1:p.Thr1859Arg
XM_017009967.1:c.5561C>G	XP_016865456.1:p.Thr1854Arg
XM_017009968.2:c.5657C>G	XP_016865457.1:p.Thr1886Arg
XM_017009969.2:c.5657C>G	XP_016865458.1:p.Thr1886Arg
XM_017009970.2:c.5657C>G	XP_016865459.1:p.Thr1886Arg
XM_017009971.2:c.5657C>G	XP_016865460.1:p.Thr1886Arg
XM_017009973.1:c.-1143C>G	XP_016865462.1:n.-1143C>G
XM_017009974.2:c.5657C>G	XP_016865463.1:p.Thr1886Arg