Canonical Allele Identifier: CA1562889900

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763391C= , CM000667.2:g.90763391C=	GRCh38
NC_000005.9:g.90059208C= , CM000667.1:g.90059208C=	GRCh37
NC_000005.8:g.90094964C=	NCBI36
NG_007083.1:g.209592C=
NG_007083.2:g.239048C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12207C= MANE Select	ENSP00000384582.2:p.Thr4069=
ENST00000425867.3:c.1161C=	ENSP00000392618.3:p.Thr387=
ENST00000639431.1:c.265+87182C=	ENSP00000491057.1:n.265+87182C=
ENST00000640464.1:n.2626C=
ENST00000640729.1:n.784C=
ENST00000405460.6:c.12207C=	ENSP00000384582.2:p.Thr4069=
NM_032119.3:c.12207C=	NP_115495.3:p.Thr4069=
NR_003149.1:n.12220C=
XM_011543675.1:c.12204C=	XP_011541977.1:p.Thr4068=
XM_011543676.1:c.12126C=	XP_011541978.1:p.Thr4042=
XM_011543677.1:c.9510C=	XP_011541979.1:p.Thr3170=
XM_011543678.1:c.12207C=	XP_011541980.1:p.Thr4069=
NM_032119.4:c.12207C= MANE Select	NP_115495.3:p.Thr4069=
XM_017009963.2:c.12228C=	XP_016865452.1:p.Thr4076=
XM_017009964.2:c.12225C=	XP_016865453.1:p.Thr4075=
XM_017009965.1:c.12225C=	XP_016865454.1:p.Thr4075=
XM_017009966.2:c.12147C=	XP_016865455.1:p.Thr4049=
XM_017009967.1:c.12132C=	XP_016865456.1:p.Thr4044=
XM_017009968.2:c.12228C=	XP_016865457.1:p.Thr4076=
XM_017009969.2:c.12228C=	XP_016865458.1:p.Thr4076=
XM_017009970.2:c.12228C=	XP_016865459.1:p.Thr4076=
XM_017009971.2:c.12228C=	XP_016865460.1:p.Thr4076=
XM_017009972.1:c.5346C=	XP_016865461.1:p.Thr1782=
XM_017009973.1:c.5325C=	XP_016865462.1:p.Thr1775=
NR_003149.2:n.12223C=