Canonical Allele Identifier: CA1562863867

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90703691A= , CM000667.2:g.90703691A=	GRCh38
NC_000005.9:g.89999508A= , CM000667.1:g.89999508A=	GRCh37
NC_000005.8:g.90035264A=	NCBI36
NG_007083.1:g.149892A=
NG_007083.2:g.179348A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.8182A= MANE Select	ENSP00000384582.2:p.Arg2728=
ENST00000639431.1:c.265+27482A=	ENSP00000491057.1:n.265+27482A=
ENST00000639473.1:n.3641A=
ENST00000640012.1:c.1989A=
ENST00000640374.1:n.1326A=
ENST00000640403.1:c.5473A=	ENSP00000492531.1:p.Arg1825=
ENST00000640779.1:c.2911A=
ENST00000405460.6:c.8182A=	ENSP00000384582.2:p.Arg2728=
ENST00000509621.1:c.879A=
NM_032119.3:c.8182A=	NP_115495.3:p.Arg2728=
NR_003149.1:n.8195A=
XM_011543675.1:c.8179A=	XP_011541977.1:p.Arg2727=
XM_011543676.1:c.8101A=	XP_011541978.1:p.Arg2701=
XM_011543677.1:c.5485A=	XP_011541979.1:p.Arg1829=
XM_011543678.1:c.8182A=	XP_011541980.1:p.Arg2728=
XM_011543679.1:c.8182A=	XP_011541981.1:p.Arg2728=
NM_032119.4:c.8182A= MANE Select	NP_115495.3:p.Arg2728=
XM_017009963.2:c.8182A=	XP_016865452.1:p.Arg2728=
XM_017009964.2:c.8179A=	XP_016865453.1:p.Arg2727=
XM_017009965.1:c.8179A=	XP_016865454.1:p.Arg2727=
XM_017009966.2:c.8101A=	XP_016865455.1:p.Arg2701=
XM_017009967.1:c.8086A=	XP_016865456.1:p.Arg2696=
XM_017009968.2:c.8182A=	XP_016865457.1:p.Arg2728=
XM_017009969.2:c.8182A=	XP_016865458.1:p.Arg2728=
XM_017009970.2:c.8182A=	XP_016865459.1:p.Arg2728=
XM_017009971.2:c.8182A=	XP_016865460.1:p.Arg2728=
XM_017009972.1:c.1300A=	XP_016865461.1:p.Arg434=
XM_017009973.1:c.1300A=	XP_016865462.1:p.Arg434=
XM_017009974.2:c.8182A=	XP_016865463.1:p.Arg2728=
NR_003149.2:n.8198A=