Canonical Allele Identifier: CA1562859328

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692782C= , CM000667.2:g.90692782C=	GRCh38
NC_000005.9:g.89988599C= , CM000667.1:g.89988599C=	GRCh37
NC_000005.8:g.90024355C=	NCBI36
NG_007083.1:g.138983C=
NG_007083.2:g.168439C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7129C= MANE Select	ENSP00000384582.2:p.Arg2377=
ENST00000639431.1:c.265+16573C=	ENSP00000491057.1:n.265+16573C=
ENST00000639473.1:n.2588C=
ENST00000640012.1:c.936C=
ENST00000640374.1:n.273C=
ENST00000640403.1:c.4420C=	ENSP00000492531.1:p.Arg1474=
ENST00000640779.1:c.1858C=
ENST00000405460.6:c.7129C=	ENSP00000384582.2:p.Arg2377=
NM_032119.3:c.7129C=	NP_115495.3:p.Arg2377=
NR_003149.1:n.7142C=
XM_011543675.1:c.7126C=	XP_011541977.1:p.Arg2376=
XM_011543676.1:c.7048C=	XP_011541978.1:p.Arg2350=
XM_011543677.1:c.4432C=	XP_011541979.1:p.Arg1478=
XM_011543678.1:c.7129C=	XP_011541980.1:p.Arg2377=
XM_011543679.1:c.7129C=	XP_011541981.1:p.Arg2377=
NM_032119.4:c.7129C= MANE Select	NP_115495.3:p.Arg2377=
XM_017009963.2:c.7129C=	XP_016865452.1:p.Arg2377=
XM_017009964.2:c.7126C=	XP_016865453.1:p.Arg2376=
XM_017009965.1:c.7126C=	XP_016865454.1:p.Arg2376=
XM_017009966.2:c.7048C=	XP_016865455.1:p.Arg2350=
XM_017009967.1:c.7033C=	XP_016865456.1:p.Arg2345=
XM_017009968.2:c.7129C=	XP_016865457.1:p.Arg2377=
XM_017009969.2:c.7129C=	XP_016865458.1:p.Arg2377=
XM_017009970.2:c.7129C=	XP_016865459.1:p.Arg2377=
XM_017009971.2:c.7129C=	XP_016865460.1:p.Arg2377=
XM_017009972.1:c.247C=	XP_016865461.1:p.Arg83=
XM_017009973.1:c.247C=	XP_016865462.1:p.Arg83=
XM_017009974.2:c.7129C=	XP_016865463.1:p.Arg2377=
NR_003149.2:n.7145C=