Canonical Allele Identifier: CA1562863857

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90703676C= , CM000667.2:g.90703676C=	GRCh38
NC_000005.9:g.89999493C= , CM000667.1:g.89999493C=	GRCh37
NC_000005.8:g.90035249C=	NCBI36
NG_007083.1:g.149877C=
NG_007083.2:g.179333C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.8167C= MANE Select	ENSP00000384582.2:p.Gln2723=
ENST00000639431.1:c.265+27467C=	ENSP00000491057.1:n.265+27467C=
ENST00000639473.1:n.3626C=
ENST00000640012.1:c.1974C=
ENST00000640374.1:n.1311C=
ENST00000640403.1:c.5458C=	ENSP00000492531.1:p.Gln1820=
ENST00000640779.1:c.2896C=
ENST00000405460.6:c.8167C=	ENSP00000384582.2:p.Gln2723=
ENST00000509621.1:c.864C=
NM_032119.3:c.8167C=	NP_115495.3:p.Gln2723=
NR_003149.1:n.8180C=
XM_011543675.1:c.8164C=	XP_011541977.1:p.Gln2722=
XM_011543676.1:c.8086C=	XP_011541978.1:p.Gln2696=
XM_011543677.1:c.5470C=	XP_011541979.1:p.Gln1824=
XM_011543678.1:c.8167C=	XP_011541980.1:p.Gln2723=
XM_011543679.1:c.8167C=	XP_011541981.1:p.Gln2723=
NM_032119.4:c.8167C= MANE Select	NP_115495.3:p.Gln2723=
XM_017009963.2:c.8167C=	XP_016865452.1:p.Gln2723=
XM_017009964.2:c.8164C=	XP_016865453.1:p.Gln2722=
XM_017009965.1:c.8164C=	XP_016865454.1:p.Gln2722=
XM_017009966.2:c.8086C=	XP_016865455.1:p.Gln2696=
XM_017009967.1:c.8071C=	XP_016865456.1:p.Gln2691=
XM_017009968.2:c.8167C=	XP_016865457.1:p.Gln2723=
XM_017009969.2:c.8167C=	XP_016865458.1:p.Gln2723=
XM_017009970.2:c.8167C=	XP_016865459.1:p.Gln2723=
XM_017009971.2:c.8167C=	XP_016865460.1:p.Gln2723=
XM_017009972.1:c.1285C=	XP_016865461.1:p.Gln429=
XM_017009973.1:c.1285C=	XP_016865462.1:p.Gln429=
XM_017009974.2:c.8167C=	XP_016865463.1:p.Gln2723=
NR_003149.2:n.8183C=