Canonical Allele Identifier: CA3132535685

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90720084G= , CM000667.2:g.90720084G=	GRCh38
NC_000005.9:g.90015901G= , CM000667.1:g.90015901G=	GRCh37
NC_000005.8:g.90051657G=	NCBI36
NG_007083.1:g.166285G=
NG_007083.2:g.195741G=

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.9484G= MANE Select	NP_115495.3:p.Glu3162=
ENST00000405460.9:c.9484G= MANE Select	ENSP00000384582.2:p.Glu3162=
NM_032119.3:c.9484G=	NP_115495.3:p.Glu3162=
NR_003149.1:n.9497G=
NR_003149.2:n.9500G=
ENST00000405460.6:c.9484G=	ENSP00000384582.2:p.Glu3162=
ENST00000509621.1:c.2181G=
ENST00000639431.1:c.265+43875G=	ENSP00000491057.1:n.265+43875G=
ENST00000640374.1:n.2628G=
ENST00000640779.1:c.4213G=
XM_011543675.1:c.9481G=	XP_011541977.1:p.Glu3161=
XM_011543676.1:c.9403G=	XP_011541978.1:p.Glu3135=
XM_011543677.1:c.6787G=	XP_011541979.1:p.Glu2263=
XM_011543678.1:c.9484G=	XP_011541980.1:p.Glu3162=
XM_011543679.1:c.9484G=	XP_011541981.1:p.Glu3162=
XM_017009963.2:c.9505G=	XP_016865452.1:p.Glu3169=
XM_017009964.2:c.9502G=	XP_016865453.1:p.Glu3168=
XM_017009965.1:c.9502G=	XP_016865454.1:p.Glu3168=
XM_017009966.2:c.9424G=	XP_016865455.1:p.Glu3142=
XM_017009967.1:c.9409G=	XP_016865456.1:p.Glu3137=
XM_017009968.2:c.9505G=	XP_016865457.1:p.Glu3169=
XM_017009969.2:c.9505G=	XP_016865458.1:p.Glu3169=
XM_017009970.2:c.9505G=	XP_016865459.1:p.Glu3169=
XM_017009971.2:c.9505G=	XP_016865460.1:p.Glu3169=
XM_017009972.1:c.2623G=	XP_016865461.1:p.Glu875=
XM_017009973.1:c.2602G=	XP_016865462.1:p.Glu868=
XM_017009974.2:c.9505G=	XP_016865463.1:p.Glu3169=
XR_001742802.1:n.2523-4275C=
XR_948560.1:n.272-4275C=