Canonical Allele Identifier: CA1562886190

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755055G= , CM000667.2:g.90755055G=	GRCh38
NC_000005.9:g.90050872G= , CM000667.1:g.90050872G=	GRCh37
NC_000005.8:g.90086628G=	NCBI36
NG_007083.1:g.201256G=
NG_007083.2:g.230712G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11450G= MANE Select	ENSP00000384582.2:p.Arg3817=
ENST00000425867.3:c.581G=	ENSP00000392618.3:p.Arg194=
ENST00000639431.1:c.265+78846G=	ENSP00000491057.1:n.265+78846G=
ENST00000640374.1:n.4594G=
ENST00000640464.1:n.1869G=
ENST00000405460.6:c.11450G=	ENSP00000384582.2:p.Arg3817=
ENST00000509621.1:c.4147G=
NM_032119.3:c.11450G=	NP_115495.3:p.Arg3817=
NR_003149.1:n.11463G=
XM_011543675.1:c.11447G=	XP_011541977.1:p.Arg3816=
XM_011543676.1:c.11369G=	XP_011541978.1:p.Arg3790=
XM_011543677.1:c.8753G=	XP_011541979.1:p.Arg2918=
XM_011543678.1:c.11450G=	XP_011541980.1:p.Arg3817=
NM_032119.4:c.11450G= MANE Select	NP_115495.3:p.Arg3817=
XM_017009963.2:c.11471G=	XP_016865452.1:p.Arg3824=
XM_017009964.2:c.11468G=	XP_016865453.1:p.Arg3823=
XM_017009965.1:c.11468G=	XP_016865454.1:p.Arg3823=
XM_017009966.2:c.11390G=	XP_016865455.1:p.Arg3797=
XM_017009967.1:c.11375G=	XP_016865456.1:p.Arg3792=
XM_017009968.2:c.11471G=	XP_016865457.1:p.Arg3824=
XM_017009969.2:c.11471G=	XP_016865458.1:p.Arg3824=
XM_017009970.2:c.11471G=	XP_016865459.1:p.Arg3824=
XM_017009971.2:c.11471G=	XP_016865460.1:p.Arg3824=
XM_017009972.1:c.4589G=	XP_016865461.1:p.Arg1530=
XM_017009973.1:c.4568G=	XP_016865462.1:p.Arg1523=
NR_003149.2:n.11466G=