Canonical Allele Identifier: CA3132535614

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90720078G= , CM000667.2:g.90720078G=	GRCh38
NC_000005.9:g.90015895G= , CM000667.1:g.90015895G=	GRCh37
NC_000005.8:g.90051651G=	NCBI36
NG_007083.1:g.166279G=
NG_007083.2:g.195735G=

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.9478G= MANE Select	NP_115495.3:p.Glu3160=
ENST00000405460.9:c.9478G= MANE Select	ENSP00000384582.2:p.Glu3160=
NM_032119.3:c.9478G=	NP_115495.3:p.Glu3160=
NR_003149.1:n.9491G=
NR_003149.2:n.9494G=
ENST00000405460.6:c.9478G=	ENSP00000384582.2:p.Glu3160=
ENST00000509621.1:c.2175G=
ENST00000639431.1:c.265+43869G=	ENSP00000491057.1:n.265+43869G=
ENST00000640374.1:n.2622G=
ENST00000640779.1:c.4207G=
XM_011543675.1:c.9475G=	XP_011541977.1:p.Glu3159=
XM_011543676.1:c.9397G=	XP_011541978.1:p.Glu3133=
XM_011543677.1:c.6781G=	XP_011541979.1:p.Glu2261=
XM_011543678.1:c.9478G=	XP_011541980.1:p.Glu3160=
XM_011543679.1:c.9478G=	XP_011541981.1:p.Glu3160=
XM_017009963.2:c.9499G=	XP_016865452.1:p.Glu3167=
XM_017009964.2:c.9496G=	XP_016865453.1:p.Glu3166=
XM_017009965.1:c.9496G=	XP_016865454.1:p.Glu3166=
XM_017009966.2:c.9418G=	XP_016865455.1:p.Glu3140=
XM_017009967.1:c.9403G=	XP_016865456.1:p.Glu3135=
XM_017009968.2:c.9499G=	XP_016865457.1:p.Glu3167=
XM_017009969.2:c.9499G=	XP_016865458.1:p.Glu3167=
XM_017009970.2:c.9499G=	XP_016865459.1:p.Glu3167=
XM_017009971.2:c.9499G=	XP_016865460.1:p.Glu3167=
XM_017009972.1:c.2617G=	XP_016865461.1:p.Glu873=
XM_017009973.1:c.2596G=	XP_016865462.1:p.Glu866=
XM_017009974.2:c.9499G=	XP_016865463.1:p.Glu3167=
XR_001742802.1:n.2523-4269C=
XR_948560.1:n.272-4269C=