Canonical Allele Identifier: CA1562886238

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755177A= , CM000667.2:g.90755177A=	GRCh38
NC_000005.9:g.90050994A= , CM000667.1:g.90050994A=	GRCh37
NC_000005.8:g.90086750A=	NCBI36
NG_007083.1:g.201378A=
NG_007083.2:g.230834A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11572A= MANE Select	ENSP00000384582.2:p.Ile3858=
ENST00000425867.3:c.703A=	ENSP00000392618.3:p.Ile235=
ENST00000639431.1:c.265+78968A=	ENSP00000491057.1:n.265+78968A=
ENST00000640374.1:n.4716A=
ENST00000640464.1:n.1991A=
ENST00000405460.6:c.11572A=	ENSP00000384582.2:p.Ile3858=
ENST00000509621.1:c.4269A=
NM_032119.3:c.11572A=	NP_115495.3:p.Ile3858=
NR_003149.1:n.11585A=
XM_011543675.1:c.11569A=	XP_011541977.1:p.Ile3857=
XM_011543676.1:c.11491A=	XP_011541978.1:p.Ile3831=
XM_011543677.1:c.8875A=	XP_011541979.1:p.Ile2959=
XM_011543678.1:c.11572A=	XP_011541980.1:p.Ile3858=
NM_032119.4:c.11572A= MANE Select	NP_115495.3:p.Ile3858=
XM_017009963.2:c.11593A=	XP_016865452.1:p.Ile3865=
XM_017009964.2:c.11590A=	XP_016865453.1:p.Ile3864=
XM_017009965.1:c.11590A=	XP_016865454.1:p.Ile3864=
XM_017009966.2:c.11512A=	XP_016865455.1:p.Ile3838=
XM_017009967.1:c.11497A=	XP_016865456.1:p.Ile3833=
XM_017009968.2:c.11593A=	XP_016865457.1:p.Ile3865=
XM_017009969.2:c.11593A=	XP_016865458.1:p.Ile3865=
XM_017009970.2:c.11593A=	XP_016865459.1:p.Ile3865=
XM_017009971.2:c.11593A=	XP_016865460.1:p.Ile3865=
XM_017009972.1:c.4711A=	XP_016865461.1:p.Ile1571=
XM_017009973.1:c.4690A=	XP_016865462.1:p.Ile1564=
NR_003149.2:n.11588A=