Canonical Allele Identifier: CA1562859317

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692752A= , CM000667.2:g.90692752A=	GRCh38
NC_000005.9:g.89988569A= , CM000667.1:g.89988569A=	GRCh37
NC_000005.8:g.90024325A=	NCBI36
NG_007083.1:g.138953A=
NG_007083.2:g.168409A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.7099A= MANE Select	ENSP00000384582.2:p.Arg2367=
ENST00000639431.1:c.265+16543A=	ENSP00000491057.1:n.265+16543A=
ENST00000639473.1:n.2558A=
ENST00000640012.1:c.906A=
ENST00000640374.1:n.243A=
ENST00000640403.1:c.4390A=	ENSP00000492531.1:p.Arg1464=
ENST00000640779.1:c.1828A=
ENST00000405460.6:c.7099A=	ENSP00000384582.2:p.Arg2367=
NM_032119.3:c.7099A=	NP_115495.3:p.Arg2367=
NR_003149.1:n.7112A=
XM_011543675.1:c.7096A=	XP_011541977.1:p.Arg2366=
XM_011543676.1:c.7018A=	XP_011541978.1:p.Arg2340=
XM_011543677.1:c.4402A=	XP_011541979.1:p.Arg1468=
XM_011543678.1:c.7099A=	XP_011541980.1:p.Arg2367=
XM_011543679.1:c.7099A=	XP_011541981.1:p.Arg2367=
NM_032119.4:c.7099A= MANE Select	NP_115495.3:p.Arg2367=
XM_017009963.2:c.7099A=	XP_016865452.1:p.Arg2367=
XM_017009964.2:c.7096A=	XP_016865453.1:p.Arg2366=
XM_017009965.1:c.7096A=	XP_016865454.1:p.Arg2366=
XM_017009966.2:c.7018A=	XP_016865455.1:p.Arg2340=
XM_017009967.1:c.7003A=	XP_016865456.1:p.Arg2335=
XM_017009968.2:c.7099A=	XP_016865457.1:p.Arg2367=
XM_017009969.2:c.7099A=	XP_016865458.1:p.Arg2367=
XM_017009970.2:c.7099A=	XP_016865459.1:p.Arg2367=
XM_017009971.2:c.7099A=	XP_016865460.1:p.Arg2367=
XM_017009972.1:c.217A=	XP_016865461.1:p.Arg73=
XM_017009973.1:c.217A=	XP_016865462.1:p.Arg73=
XM_017009974.2:c.7099A=	XP_016865463.1:p.Arg2367=
NR_003149.2:n.7115A=