Canonical Allele Identifier: CA246399

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90753609C>A , CM000667.2:g.90753609C>A	GRCh38
NC_000005.9:g.90049426C>A , CM000667.1:g.90049426C>A	GRCh37
NC_000005.8:g.90085182C>A	NCBI36
NG_007083.1:g.199810C>A
NG_007083.2:g.229266C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.11157C>A MANE Select	NP_115495.3:p.Ile3719=
ENST00000405460.9:c.11157C>A MANE Select	ENSP00000384582.2:p.Ile3719=
NM_032119.3:c.11157C>A	NP_115495.3:p.Ile3719=
NR_003149.1:n.11170C>A
NR_003149.2:n.11173C>A
ENST00000405460.6:c.11157C>A	ENSP00000384582.2:p.Ile3719=
ENST00000425867.3:c.288C>A	ENSP00000392618.3:p.Ile96=
ENST00000509621.1:c.3854C>A
ENST00000639431.1:c.265+77400C>A	ENSP00000491057.1:n.265+77400C>A
ENST00000640374.1:n.4301C>A
ENST00000640464.1:n.1576C>A
XM_011543675.1:c.11154C>A	XP_011541977.1:p.Ile3718=
XM_011543676.1:c.11076C>A	XP_011541978.1:p.Ile3692=
XM_011543677.1:c.8460C>A	XP_011541979.1:p.Ile2820=
XM_011543678.1:c.11157C>A	XP_011541980.1:p.Ile3719=
XM_017009963.2:c.11178C>A	XP_016865452.1:p.Ile3726=
XM_017009964.2:c.11175C>A	XP_016865453.1:p.Ile3725=
XM_017009965.1:c.11175C>A	XP_016865454.1:p.Ile3725=
XM_017009966.2:c.11097C>A	XP_016865455.1:p.Ile3699=
XM_017009967.1:c.11082C>A	XP_016865456.1:p.Ile3694=
XM_017009968.2:c.11178C>A	XP_016865457.1:p.Ile3726=
XM_017009969.2:c.11178C>A	XP_016865458.1:p.Ile3726=
XM_017009970.2:c.11178C>A	XP_016865459.1:p.Ile3726=
XM_017009971.2:c.11178C>A	XP_016865460.1:p.Ile3726=
XM_017009972.1:c.4296C>A	XP_016865461.1:p.Ile1432=
XM_017009973.1:c.4275C>A	XP_016865462.1:p.Ile1425=