Canonical Allele Identifier: CA1562889910

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763410A= , CM000667.2:g.90763410A=	GRCh38
NC_000005.9:g.90059227A= , CM000667.1:g.90059227A=	GRCh37
NC_000005.8:g.90094983A=	NCBI36
NG_007083.1:g.209611A=
NG_007083.2:g.239067A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12226A= MANE Select	ENSP00000384582.2:p.Ile4076=
ENST00000425867.3:c.1180A=	ENSP00000392618.3:p.Ile394=
ENST00000639431.1:c.265+87201A=	ENSP00000491057.1:n.265+87201A=
ENST00000640464.1:n.2645A=
ENST00000640729.1:n.803A=
ENST00000405460.6:c.12226A=	ENSP00000384582.2:p.Ile4076=
NM_032119.3:c.12226A=	NP_115495.3:p.Ile4076=
NR_003149.1:n.12239A=
XM_011543675.1:c.12223A=	XP_011541977.1:p.Ile4075=
XM_011543676.1:c.12145A=	XP_011541978.1:p.Ile4049=
XM_011543677.1:c.9529A=	XP_011541979.1:p.Ile3177=
XM_011543678.1:c.12226A=	XP_011541980.1:p.Ile4076=
NM_032119.4:c.12226A= MANE Select	NP_115495.3:p.Ile4076=
XM_017009963.2:c.12247A=	XP_016865452.1:p.Ile4083=
XM_017009964.2:c.12244A=	XP_016865453.1:p.Ile4082=
XM_017009965.1:c.12244A=	XP_016865454.1:p.Ile4082=
XM_017009966.2:c.12166A=	XP_016865455.1:p.Ile4056=
XM_017009967.1:c.12151A=	XP_016865456.1:p.Ile4051=
XM_017009968.2:c.12247A=	XP_016865457.1:p.Ile4083=
XM_017009969.2:c.12247A=	XP_016865458.1:p.Ile4083=
XM_017009970.2:c.12247A=	XP_016865459.1:p.Ile4083=
XM_017009971.2:c.12247A=	XP_016865460.1:p.Ile4083=
XM_017009972.1:c.5365A=	XP_016865461.1:p.Ile1789=
XM_017009973.1:c.5344A=	XP_016865462.1:p.Ile1782=
NR_003149.2:n.12242A=