Canonical Allele Identifier: CA1562867531

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712321A= , CM000667.2:g.90712321A=	GRCh38
NC_000005.9:g.90008138A= , CM000667.1:g.90008138A=	GRCh37
NC_000005.8:g.90043894A=	NCBI36
NG_007083.1:g.158522A=
NG_007083.2:g.187978A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9077A= MANE Select	ENSP00000384582.2:p.Asn3026=
ENST00000639431.1:c.265+36112A=	ENSP00000491057.1:n.265+36112A=
ENST00000639473.1:n.4536A=
ENST00000640012.1:c.2884A=
ENST00000640374.1:n.2221A=
ENST00000640779.1:c.3806A=
ENST00000405460.6:c.9077A=	ENSP00000384582.2:p.Asn3026=
ENST00000509621.1:c.1774A=
NM_032119.3:c.9077A=	NP_115495.3:p.Asn3026=
NR_003149.1:n.9090A=
XM_011543675.1:c.9074A=	XP_011541977.1:p.Asn3025=
XM_011543676.1:c.8996A=	XP_011541978.1:p.Asn2999=
XM_011543677.1:c.6380A=	XP_011541979.1:p.Asn2127=
XM_011543678.1:c.9077A=	XP_011541980.1:p.Asn3026=
XM_011543679.1:c.9077A=	XP_011541981.1:p.Asn3026=
NM_032119.4:c.9077A= MANE Select	NP_115495.3:p.Asn3026=
XM_017009963.2:c.9098A=	XP_016865452.1:p.Asn3033=
XM_017009964.2:c.9095A=	XP_016865453.1:p.Asn3032=
XM_017009965.1:c.9095A=	XP_016865454.1:p.Asn3032=
XM_017009966.2:c.9017A=	XP_016865455.1:p.Asn3006=
XM_017009967.1:c.9002A=	XP_016865456.1:p.Asn3001=
XM_017009968.2:c.9098A=	XP_016865457.1:p.Asn3033=
XM_017009969.2:c.9098A=	XP_016865458.1:p.Asn3033=
XM_017009970.2:c.9098A=	XP_016865459.1:p.Asn3033=
XM_017009971.2:c.9098A=	XP_016865460.1:p.Asn3033=
XM_017009972.1:c.2216A=	XP_016865461.1:p.Asn739=
XM_017009973.1:c.2195A=	XP_016865462.1:p.Asn732=
XM_017009974.2:c.9098A=	XP_016865463.1:p.Asn3033=
NR_003149.2:n.9093A=