Canonical Allele Identifier: CA1562895808

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90776485C= , CM000667.2:g.90776485C=	GRCh38
NC_000005.9:g.90072302C= , CM000667.1:g.90072302C=	GRCh37
NC_000005.8:g.90108058C=	NCBI36
NG_007083.1:g.222686C=
NG_007083.2:g.252142C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12436C= MANE Select	ENSP00000384582.2:p.Arg4146=
ENST00000425867.3:c.1390C=	ENSP00000392618.3:p.Arg464=
ENST00000639431.1:c.265+100276C=	ENSP00000491057.1:n.265+100276C=
ENST00000640464.1:n.2855C=
ENST00000640729.1:n.1013C=
ENST00000405460.6:c.12436C=	ENSP00000384582.2:p.Arg4146=
NM_032119.3:c.12436C=	NP_115495.3:p.Arg4146=
NR_003149.1:n.12449C=
XM_011543675.1:c.12433C=	XP_011541977.1:p.Arg4145=
XM_011543676.1:c.12355C=	XP_011541978.1:p.Arg4119=
XM_011543677.1:c.9739C=	XP_011541979.1:p.Arg3247=
XM_011543678.1:c.12436C=	XP_011541980.1:p.Arg4146=
NM_032119.4:c.12436C= MANE Select	NP_115495.3:p.Arg4146=
XM_017009963.2:c.12457C=	XP_016865452.1:p.Arg4153=
XM_017009964.2:c.12454C=	XP_016865453.1:p.Arg4152=
XM_017009965.1:c.12454C=	XP_016865454.1:p.Arg4152=
XM_017009966.2:c.12376C=	XP_016865455.1:p.Arg4126=
XM_017009967.1:c.12361C=	XP_016865456.1:p.Arg4121=
XM_017009968.2:c.12457C=	XP_016865457.1:p.Arg4153=
XM_017009969.2:c.12457C=	XP_016865458.1:p.Arg4153=
XM_017009970.2:c.12457C=	XP_016865459.1:p.Arg4153=
XM_017009971.2:c.12457C=	XP_016865460.1:p.Arg4153=
XM_017009972.1:c.5575C=	XP_016865461.1:p.Arg1859=
XM_017009973.1:c.5554C=	XP_016865462.1:p.Arg1852=
NR_003149.2:n.12452C=