Canonical Allele Identifier: CA1562889881

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763355A= , CM000667.2:g.90763355A=	GRCh38
NC_000005.9:g.90059172A= , CM000667.1:g.90059172A=	GRCh37
NC_000005.8:g.90094928A=	NCBI36
NG_007083.1:g.209556A=
NG_007083.2:g.239012A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12171A= MANE Select	ENSP00000384582.2:p.Thr4057=
ENST00000425867.3:c.1125A=	ENSP00000392618.3:p.Thr375=
ENST00000639431.1:c.265+87146A=	ENSP00000491057.1:n.265+87146A=
ENST00000640464.1:n.2590A=
ENST00000640729.1:n.748A=
ENST00000405460.6:c.12171A=	ENSP00000384582.2:p.Thr4057=
NM_032119.3:c.12171A=	NP_115495.3:p.Thr4057=
NR_003149.1:n.12184A=
XM_011543675.1:c.12168A=	XP_011541977.1:p.Thr4056=
XM_011543676.1:c.12090A=	XP_011541978.1:p.Thr4030=
XM_011543677.1:c.9474A=	XP_011541979.1:p.Thr3158=
XM_011543678.1:c.12171A=	XP_011541980.1:p.Thr4057=
NM_032119.4:c.12171A= MANE Select	NP_115495.3:p.Thr4057=
XM_017009963.2:c.12192A=	XP_016865452.1:p.Thr4064=
XM_017009964.2:c.12189A=	XP_016865453.1:p.Thr4063=
XM_017009965.1:c.12189A=	XP_016865454.1:p.Thr4063=
XM_017009966.2:c.12111A=	XP_016865455.1:p.Thr4037=
XM_017009967.1:c.12096A=	XP_016865456.1:p.Thr4032=
XM_017009968.2:c.12192A=	XP_016865457.1:p.Thr4064=
XM_017009969.2:c.12192A=	XP_016865458.1:p.Thr4064=
XM_017009970.2:c.12192A=	XP_016865459.1:p.Thr4064=
XM_017009971.2:c.12192A=	XP_016865460.1:p.Thr4064=
XM_017009972.1:c.5310A=	XP_016865461.1:p.Thr1770=
XM_017009973.1:c.5289A=	XP_016865462.1:p.Thr1763=
NR_003149.2:n.12187A=