Canonical Allele Identifier: CA1562863821

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90703588G= , CM000667.2:g.90703588G=	GRCh38
NC_000005.9:g.89999405G= , CM000667.1:g.89999405G=	GRCh37
NC_000005.8:g.90035161G=	NCBI36
NG_007083.1:g.149789G=
NG_007083.2:g.179245G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.8156-77G= MANE Select	ENSP00000384582.2:n.8156-77G=
ENST00000639431.1:c.265+27379G=	ENSP00000491057.1:n.265+27379G=
ENST00000639473.1:n.3615-77G=
ENST00000640012.1:c.1963-77G=
ENST00000640374.1:n.1300-77G=
ENST00000640403.1:c.5447-77G=	ENSP00000492531.1:n.5447-77G=
ENST00000640779.1:c.2885-77G=
ENST00000405460.6:c.8156-77G=	ENSP00000384582.2:n.8156-77G=
ENST00000509621.1:c.853-77G=
NM_032119.3:c.8156-77G=	NP_115495.3:n.8156-77G=
NR_003149.1:n.8169-77G=
XM_011543675.1:c.8153-77G=	XP_011541977.1:n.8153-77G=
XM_011543676.1:c.8075-77G=	XP_011541978.1:n.8075-77G=
XM_011543677.1:c.5459-77G=	XP_011541979.1:n.5459-77G=
XM_011543678.1:c.8156-77G=	XP_011541980.1:n.8156-77G=
XM_011543679.1:c.8156-77G=	XP_011541981.1:n.8156-77G=
NM_032119.4:c.8156-77G= MANE Select	NP_115495.3:n.8156-77G=
XM_017009963.2:c.8156-77G=	XP_016865452.1:n.8156-77G=
XM_017009964.2:c.8153-77G=	XP_016865453.1:n.8153-77G=
XM_017009965.1:c.8153-77G=	XP_016865454.1:n.8153-77G=
XM_017009966.2:c.8075-77G=	XP_016865455.1:n.8075-77G=
XM_017009967.1:c.8060-77G=	XP_016865456.1:n.8060-77G=
XM_017009968.2:c.8156-77G=	XP_016865457.1:n.8156-77G=
XM_017009969.2:c.8156-77G=	XP_016865458.1:n.8156-77G=
XM_017009970.2:c.8156-77G=	XP_016865459.1:n.8156-77G=
XM_017009971.2:c.8156-77G=	XP_016865460.1:n.8156-77G=
XM_017009972.1:c.1274-77G=	XP_016865461.1:n.1274-77G=
XM_017009973.1:c.1274-77G=	XP_016865462.1:n.1274-77G=
XM_017009974.2:c.8156-77G=	XP_016865463.1:n.8156-77G=
NR_003149.2:n.8172-77G=