Canonical Allele Identifier: CA1562908497

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90811000G= , CM000667.2:g.90811000G=	GRCh38
NC_000005.9:g.90106817G= , CM000667.1:g.90106817G=	GRCh37
NC_000005.8:g.90142573G=	NCBI36
NG_007083.1:g.257201G=
NG_007083.2:g.286657G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.15740G= MANE Select	ENSP00000384582.2:p.Arg5247=
ENST00000425867.3:c.4694G=	ENSP00000392618.3:p.Arg1565=
ENST00000638510.1:n.3007G=
ENST00000639431.1:c.265+134791G=	ENSP00000491057.1:n.265+134791G=
ENST00000640407.1:c.2150G=	ENSP00000491425.1:p.Arg717=
ENST00000405460.6:c.15740G=	ENSP00000384582.2:p.Arg5247=
ENST00000425867.2:c.2723G=	ENSP00000392618.2:p.Arg908=
NM_032119.3:c.15740G=	NP_115495.3:p.Arg5247=
NR_003149.1:n.15753G=
XM_011543675.1:c.15737G=	XP_011541977.1:p.Arg5246=
XM_011543676.1:c.15659G=	XP_011541978.1:p.Arg5220=
XM_011543677.1:c.13043G=	XP_011541979.1:p.Arg4348=
NM_032119.4:c.15740G= MANE Select	NP_115495.3:p.Arg5247=
XM_017009963.2:c.15761G=	XP_016865452.1:p.Arg5254=
XM_017009964.2:c.15758G=	XP_016865453.1:p.Arg5253=
XM_017009965.1:c.15758G=	XP_016865454.1:p.Arg5253=
XM_017009966.2:c.15680G=	XP_016865455.1:p.Arg5227=
XM_017009967.1:c.15665G=	XP_016865456.1:p.Arg5222=
XM_017009968.2:c.15581G=	XP_016865457.1:p.Arg5194=
XM_017009969.2:c.15761G=	XP_016865458.1:p.Arg5254=
XM_017009972.1:c.8879G=	XP_016865461.1:p.Arg2960=
XM_017009973.1:c.8858G=	XP_016865462.1:p.Arg2953=
NR_003149.2:n.15756G=