Canonical Allele Identifier: CA3341679

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90790986A>G , CM000667.2:g.90790986A>G	GRCh38
NC_000005.9:g.90086803A>G , CM000667.1:g.90086803A>G	GRCh37
NC_000005.8:g.90122559A>G	NCBI36
NG_007083.1:g.237187A>G
NG_007083.2:g.266643A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14157A>G MANE Select	ENSP00000384582.2:p.Leu4719=
ENST00000425867.3:c.3111A>G	ENSP00000392618.3:p.Leu1037=
ENST00000638510.1:n.1424A>G
ENST00000638975.1:c.786A>G	ENSP00000492630.1:p.Leu262=
ENST00000639431.1:c.265+114777A>G	ENSP00000491057.1:n.265+114777A>G
ENST00000640407.1:c.567A>G	ENSP00000491425.1:p.Leu189=
ENST00000405460.6:c.14157A>G	ENSP00000384582.2:p.Leu4719=
ENST00000425867.2:c.1140A>G	ENSP00000392618.2:p.Leu380=
NM_032119.3:c.14157A>G	NP_115495.3:p.Leu4719=
NR_003149.1:n.14170A>G
XM_011543675.1:c.14154A>G	XP_011541977.1:p.Leu4718=
XM_011543676.1:c.14076A>G	XP_011541978.1:p.Leu4692=
XM_011543677.1:c.11460A>G	XP_011541979.1:p.Leu3820=
XM_011543678.1:c.14157A>G	XP_011541980.1:p.Leu4719=
NM_032119.4:c.14157A>G MANE Select	NP_115495.3:p.Leu4719=
XM_017009963.2:c.14178A>G	XP_016865452.1:p.Leu4726=
XM_017009964.2:c.14175A>G	XP_016865453.1:p.Leu4725=
XM_017009965.1:c.14175A>G	XP_016865454.1:p.Leu4725=
XM_017009966.2:c.14097A>G	XP_016865455.1:p.Leu4699=
XM_017009967.1:c.14082A>G	XP_016865456.1:p.Leu4694=
XM_017009968.2:c.14178A>G	XP_016865457.1:p.Leu4726=
XM_017009969.2:c.14178A>G	XP_016865458.1:p.Leu4726=
XM_017009970.2:c.14178A>G	XP_016865459.1:p.Leu4726=
XM_017009971.2:c.14178A>G	XP_016865460.1:p.Leu4726=
XM_017009972.1:c.7296A>G	XP_016865461.1:p.Leu2432=
XM_017009973.1:c.7275A>G	XP_016865462.1:p.Leu2425=
NR_003149.2:n.14173A>G