Canonical Allele Identifier: CA1562886213

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755123G= , CM000667.2:g.90755123G=	GRCh38
NC_000005.9:g.90050940G= , CM000667.1:g.90050940G=	GRCh37
NC_000005.8:g.90086696G=	NCBI36
NG_007083.1:g.201324G=
NG_007083.2:g.230780G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11518G= MANE Select	ENSP00000384582.2:p.Glu3840=
ENST00000425867.3:c.649G=	ENSP00000392618.3:p.Glu217=
ENST00000639431.1:c.265+78914G=	ENSP00000491057.1:n.265+78914G=
ENST00000640374.1:n.4662G=
ENST00000640464.1:n.1937G=
ENST00000405460.6:c.11518G=	ENSP00000384582.2:p.Glu3840=
ENST00000509621.1:c.4215G=
NM_032119.3:c.11518G=	NP_115495.3:p.Glu3840=
NR_003149.1:n.11531G=
XM_011543675.1:c.11515G=	XP_011541977.1:p.Glu3839=
XM_011543676.1:c.11437G=	XP_011541978.1:p.Glu3813=
XM_011543677.1:c.8821G=	XP_011541979.1:p.Glu2941=
XM_011543678.1:c.11518G=	XP_011541980.1:p.Glu3840=
NM_032119.4:c.11518G= MANE Select	NP_115495.3:p.Glu3840=
XM_017009963.2:c.11539G=	XP_016865452.1:p.Glu3847=
XM_017009964.2:c.11536G=	XP_016865453.1:p.Glu3846=
XM_017009965.1:c.11536G=	XP_016865454.1:p.Glu3846=
XM_017009966.2:c.11458G=	XP_016865455.1:p.Glu3820=
XM_017009967.1:c.11443G=	XP_016865456.1:p.Glu3815=
XM_017009968.2:c.11539G=	XP_016865457.1:p.Glu3847=
XM_017009969.2:c.11539G=	XP_016865458.1:p.Glu3847=
XM_017009970.2:c.11539G=	XP_016865459.1:p.Glu3847=
XM_017009971.2:c.11539G=	XP_016865460.1:p.Glu3847=
XM_017009972.1:c.4657G=	XP_016865461.1:p.Glu1553=
XM_017009973.1:c.4636G=	XP_016865462.1:p.Glu1546=
NR_003149.2:n.11534G=