Canonical Allele Identifier: CA1562867563

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712413G= , CM000667.2:g.90712413G=	GRCh38
NC_000005.9:g.90008230G= , CM000667.1:g.90008230G=	GRCh37
NC_000005.8:g.90043986G=	NCBI36
NG_007083.1:g.158614G=
NG_007083.2:g.188070G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9169G= MANE Select	ENSP00000384582.2:p.Gly3057=
ENST00000639431.1:c.265+36204G=	ENSP00000491057.1:n.265+36204G=
ENST00000639473.1:n.4628G=
ENST00000640012.1:c.2976G=
ENST00000640374.1:n.2313G=
ENST00000640779.1:c.3898G=
ENST00000405460.6:c.9169G=	ENSP00000384582.2:p.Gly3057=
ENST00000509621.1:c.1866G=
NM_032119.3:c.9169G=	NP_115495.3:p.Gly3057=
NR_003149.1:n.9182G=
XM_011543675.1:c.9166G=	XP_011541977.1:p.Gly3056=
XM_011543676.1:c.9088G=	XP_011541978.1:p.Gly3030=
XM_011543677.1:c.6472G=	XP_011541979.1:p.Gly2158=
XM_011543678.1:c.9169G=	XP_011541980.1:p.Gly3057=
XM_011543679.1:c.9169G=	XP_011541981.1:p.Gly3057=
XR_948560.1:n.437-4C=
NM_032119.4:c.9169G= MANE Select	NP_115495.3:p.Gly3057=
XM_017009963.2:c.9190G=	XP_016865452.1:p.Gly3064=
XM_017009964.2:c.9187G=	XP_016865453.1:p.Gly3063=
XM_017009965.1:c.9187G=	XP_016865454.1:p.Gly3063=
XM_017009966.2:c.9109G=	XP_016865455.1:p.Gly3037=
XM_017009967.1:c.9094G=	XP_016865456.1:p.Gly3032=
XM_017009968.2:c.9190G=	XP_016865457.1:p.Gly3064=
XM_017009969.2:c.9190G=	XP_016865458.1:p.Gly3064=
XM_017009970.2:c.9190G=	XP_016865459.1:p.Gly3064=
XM_017009971.2:c.9190G=	XP_016865460.1:p.Gly3064=
XM_017009972.1:c.2308G=	XP_016865461.1:p.Gly770=
XM_017009973.1:c.2287G=	XP_016865462.1:p.Gly763=
XM_017009974.2:c.9190G=	XP_016865463.1:p.Gly3064=
NR_003149.2:n.9185G=