Canonical Allele Identifier: CA1562867542

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712362G= , CM000667.2:g.90712362G=	GRCh38
NC_000005.9:g.90008179G= , CM000667.1:g.90008179G=	GRCh37
NC_000005.8:g.90043935G=	NCBI36
NG_007083.1:g.158563G=
NG_007083.2:g.188019G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9118G= MANE Select	ENSP00000384582.2:p.Asp3040=
ENST00000639431.1:c.265+36153G=	ENSP00000491057.1:n.265+36153G=
ENST00000639473.1:n.4577G=
ENST00000640012.1:c.2925G=
ENST00000640374.1:n.2262G=
ENST00000640779.1:c.3847G=
ENST00000405460.6:c.9118G=	ENSP00000384582.2:p.Asp3040=
ENST00000509621.1:c.1815G=
NM_032119.3:c.9118G=	NP_115495.3:p.Asp3040=
NR_003149.1:n.9131G=
XM_011543675.1:c.9115G=	XP_011541977.1:p.Asp3039=
XM_011543676.1:c.9037G=	XP_011541978.1:p.Asp3013=
XM_011543677.1:c.6421G=	XP_011541979.1:p.Asp2141=
XM_011543678.1:c.9118G=	XP_011541980.1:p.Asp3040=
XM_011543679.1:c.9118G=	XP_011541981.1:p.Asp3040=
NM_032119.4:c.9118G= MANE Select	NP_115495.3:p.Asp3040=
XM_017009963.2:c.9139G=	XP_016865452.1:p.Asp3047=
XM_017009964.2:c.9136G=	XP_016865453.1:p.Asp3046=
XM_017009965.1:c.9136G=	XP_016865454.1:p.Asp3046=
XM_017009966.2:c.9058G=	XP_016865455.1:p.Asp3020=
XM_017009967.1:c.9043G=	XP_016865456.1:p.Asp3015=
XM_017009968.2:c.9139G=	XP_016865457.1:p.Asp3047=
XM_017009969.2:c.9139G=	XP_016865458.1:p.Asp3047=
XM_017009970.2:c.9139G=	XP_016865459.1:p.Asp3047=
XM_017009971.2:c.9139G=	XP_016865460.1:p.Asp3047=
XM_017009972.1:c.2257G=	XP_016865461.1:p.Asp753=
XM_017009973.1:c.2236G=	XP_016865462.1:p.Asp746=
XM_017009974.2:c.9139G=	XP_016865463.1:p.Asp3047=
NR_003149.2:n.9134G=