Canonical Allele Identifier: CA1562882078

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745634A= , CM000667.2:g.90745634A=	GRCh38
NC_000005.9:g.90041451A= , CM000667.1:g.90041451A=	GRCh37
NC_000005.8:g.90077207A=	NCBI36
NG_007083.1:g.191835A=
NG_007083.2:g.221291A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10813A= MANE Select	ENSP00000384582.2:p.Ile3605=
ENST00000639431.1:c.265+69425A=	ENSP00000491057.1:n.265+69425A=
ENST00000640374.1:n.3957A=
ENST00000640464.1:n.1232A=
ENST00000405460.6:c.10813A=	ENSP00000384582.2:p.Ile3605=
ENST00000509621.1:c.3510A=
NM_032119.3:c.10813A=	NP_115495.3:p.Ile3605=
NR_003149.1:n.10826A=
XM_011543675.1:c.10810A=	XP_011541977.1:p.Ile3604=
XM_011543676.1:c.10732A=	XP_011541978.1:p.Ile3578=
XM_011543677.1:c.8116A=	XP_011541979.1:p.Ile2706=
XM_011543678.1:c.10813A=	XP_011541980.1:p.Ile3605=
XM_011543679.1:c.*35A=	XP_011541981.1:n.*35A=
NM_032119.4:c.10813A= MANE Select	NP_115495.3:p.Ile3605=
XM_017009963.2:c.10834A=	XP_016865452.1:p.Ile3612=
XM_017009964.2:c.10831A=	XP_016865453.1:p.Ile3611=
XM_017009965.1:c.10831A=	XP_016865454.1:p.Ile3611=
XM_017009966.2:c.10753A=	XP_016865455.1:p.Ile3585=
XM_017009967.1:c.10738A=	XP_016865456.1:p.Ile3580=
XM_017009968.2:c.10834A=	XP_016865457.1:p.Ile3612=
XM_017009969.2:c.10834A=	XP_016865458.1:p.Ile3612=
XM_017009970.2:c.10834A=	XP_016865459.1:p.Ile3612=
XM_017009971.2:c.10834A=	XP_016865460.1:p.Ile3612=
XM_017009972.1:c.3952A=	XP_016865461.1:p.Ile1318=
XM_017009973.1:c.3931A=	XP_016865462.1:p.Ile1311=
XM_017009974.2:c.*35A=	XP_016865463.1:n.*35A=
NR_003149.2:n.10829A=