Canonical Allele Identifier: CA3338981

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90643909A>G , CM000667.2:g.90643909A>G	GRCh38
NC_000005.9:g.89939726A>G , CM000667.1:g.89939726A>G	GRCh37
NC_000005.8:g.89975482A>G	NCBI36
NG_007083.1:g.90110A>G
NG_007083.2:g.119566A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.2660A>G MANE Select	NP_115495.3:p.His887Arg
ENST00000405460.9:c.2660A>G MANE Select	ENSP00000384582.2:p.His887Arg
NM_032119.3:c.2660A>G	NP_115495.3:p.His887Arg
NR_003149.1:n.2756A>G
NR_003149.2:n.2759A>G
ENST00000405460.6:c.2660A>G	ENSP00000384582.2:p.His887Arg
ENST00000504142.1:c.1425A>G
ENST00000504142.2:n.1426A>G
ENST00000512205.1:n.570A>G
ENST00000639676.1:n.258A>G
ENST00000640403.1:c.-38A>G	ENSP00000492531.1:n.-38A>G
XM_011543675.1:c.2660A>G	XP_011541977.1:p.His887Arg
XM_011543676.1:c.2660A>G	XP_011541978.1:p.His887Arg
XM_011543677.1:c.-38A>G	XP_011541979.1:n.-38A>G
XM_011543678.1:c.2660A>G	XP_011541980.1:p.His887Arg
XM_011543679.1:c.2660A>G	XP_011541981.1:p.His887Arg
XM_017009963.2:c.2660A>G	XP_016865452.1:p.His887Arg
XM_017009964.2:c.2660A>G	XP_016865453.1:p.His887Arg
XM_017009965.1:c.2657A>G	XP_016865454.1:p.His886Arg
XM_017009966.2:c.2660A>G	XP_016865455.1:p.His887Arg
XM_017009967.1:c.2564A>G	XP_016865456.1:p.His855Arg
XM_017009968.2:c.2660A>G	XP_016865457.1:p.His887Arg
XM_017009969.2:c.2660A>G	XP_016865458.1:p.His887Arg
XM_017009970.2:c.2660A>G	XP_016865459.1:p.His887Arg
XM_017009971.2:c.2660A>G	XP_016865460.1:p.His887Arg
XM_017009974.2:c.2660A>G	XP_016865463.1:p.His887Arg