Canonical Allele Identifier: CA1562886157

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90754984A= , CM000667.2:g.90754984A=	GRCh38
NC_000005.9:g.90050801A= , CM000667.1:g.90050801A=	GRCh37
NC_000005.8:g.90086557A=	NCBI36
NG_007083.1:g.201185A=
NG_007083.2:g.230641A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11379A= MANE Select	ENSP00000384582.2:p.Glu3793=
ENST00000425867.3:c.510A=	ENSP00000392618.3:p.Glu170=
ENST00000639431.1:c.265+78775A=	ENSP00000491057.1:n.265+78775A=
ENST00000640374.1:n.4523A=
ENST00000640464.1:n.1798A=
ENST00000405460.6:c.11379A=	ENSP00000384582.2:p.Glu3793=
ENST00000509621.1:c.4076A=
NM_032119.3:c.11379A=	NP_115495.3:p.Glu3793=
NR_003149.1:n.11392A=
XM_011543675.1:c.11376A=	XP_011541977.1:p.Glu3792=
XM_011543676.1:c.11298A=	XP_011541978.1:p.Glu3766=
XM_011543677.1:c.8682A=	XP_011541979.1:p.Glu2894=
XM_011543678.1:c.11379A=	XP_011541980.1:p.Glu3793=
NM_032119.4:c.11379A= MANE Select	NP_115495.3:p.Glu3793=
XM_017009963.2:c.11400A=	XP_016865452.1:p.Glu3800=
XM_017009964.2:c.11397A=	XP_016865453.1:p.Glu3799=
XM_017009965.1:c.11397A=	XP_016865454.1:p.Glu3799=
XM_017009966.2:c.11319A=	XP_016865455.1:p.Glu3773=
XM_017009967.1:c.11304A=	XP_016865456.1:p.Glu3768=
XM_017009968.2:c.11400A=	XP_016865457.1:p.Glu3800=
XM_017009969.2:c.11400A=	XP_016865458.1:p.Glu3800=
XM_017009970.2:c.11400A=	XP_016865459.1:p.Glu3800=
XM_017009971.2:c.11400A=	XP_016865460.1:p.Glu3800=
XM_017009972.1:c.4518A=	XP_016865461.1:p.Glu1506=
XM_017009973.1:c.4497A=	XP_016865462.1:p.Glu1499=
NR_003149.2:n.11395A=