Canonical Allele Identifier: CA1562886171

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755015C= , CM000667.2:g.90755015C=	GRCh38
NC_000005.9:g.90050832C= , CM000667.1:g.90050832C=	GRCh37
NC_000005.8:g.90086588C=	NCBI36
NG_007083.1:g.201216C=
NG_007083.2:g.230672C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11410C= MANE Select	ENSP00000384582.2:p.Arg3804=
ENST00000425867.3:c.541C=	ENSP00000392618.3:p.Arg181=
ENST00000639431.1:c.265+78806C=	ENSP00000491057.1:n.265+78806C=
ENST00000640374.1:n.4554C=
ENST00000640464.1:n.1829C=
ENST00000405460.6:c.11410C=	ENSP00000384582.2:p.Arg3804=
ENST00000509621.1:c.4107C=
NM_032119.3:c.11410C=	NP_115495.3:p.Arg3804=
NR_003149.1:n.11423C=
XM_011543675.1:c.11407C=	XP_011541977.1:p.Arg3803=
XM_011543676.1:c.11329C=	XP_011541978.1:p.Arg3777=
XM_011543677.1:c.8713C=	XP_011541979.1:p.Arg2905=
XM_011543678.1:c.11410C=	XP_011541980.1:p.Arg3804=
NM_032119.4:c.11410C= MANE Select	NP_115495.3:p.Arg3804=
XM_017009963.2:c.11431C=	XP_016865452.1:p.Arg3811=
XM_017009964.2:c.11428C=	XP_016865453.1:p.Arg3810=
XM_017009965.1:c.11428C=	XP_016865454.1:p.Arg3810=
XM_017009966.2:c.11350C=	XP_016865455.1:p.Arg3784=
XM_017009967.1:c.11335C=	XP_016865456.1:p.Arg3779=
XM_017009968.2:c.11431C=	XP_016865457.1:p.Arg3811=
XM_017009969.2:c.11431C=	XP_016865458.1:p.Arg3811=
XM_017009970.2:c.11431C=	XP_016865459.1:p.Arg3811=
XM_017009971.2:c.11431C=	XP_016865460.1:p.Arg3811=
XM_017009972.1:c.4549C=	XP_016865461.1:p.Arg1517=
XM_017009973.1:c.4528C=	XP_016865462.1:p.Arg1510=
NR_003149.2:n.11426C=