Canonical Allele Identifier: CA1562836947

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90644869G= , CM000667.2:g.90644869G=	GRCh38
NC_000005.9:g.89940686G= , CM000667.1:g.89940686G=	GRCh37
NC_000005.8:g.89976442G=	NCBI36
NG_007083.1:g.91070G=
NG_007083.2:g.120526G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.2898G= MANE Select	ENSP00000384582.2:p.Glu966=
ENST00000504142.2:n.1664G=
ENST00000639676.1:n.496G=
ENST00000640403.1:c.201G=	ENSP00000492531.1:p.Glu67=
ENST00000405460.6:c.2898G=	ENSP00000384582.2:p.Glu966=
ENST00000504142.1:c.1663G=
NM_032119.3:c.2898G=	NP_115495.3:p.Glu966=
NR_003149.1:n.2994G=
XM_011543675.1:c.2898G=	XP_011541977.1:p.Glu966=
XM_011543676.1:c.2898G=	XP_011541978.1:p.Glu966=
XM_011543677.1:c.201G=	XP_011541979.1:p.Glu67=
XM_011543678.1:c.2898G=	XP_011541980.1:p.Glu966=
XM_011543679.1:c.2898G=	XP_011541981.1:p.Glu966=
NM_032119.4:c.2898G= MANE Select	NP_115495.3:p.Glu966=
XM_017009963.2:c.2898G=	XP_016865452.1:p.Glu966=
XM_017009964.2:c.2898G=	XP_016865453.1:p.Glu966=
XM_017009965.1:c.2895G=	XP_016865454.1:p.Glu965=
XM_017009966.2:c.2898G=	XP_016865455.1:p.Glu966=
XM_017009967.1:c.2802G=	XP_016865456.1:p.Glu934=
XM_017009968.2:c.2898G=	XP_016865457.1:p.Glu966=
XM_017009969.2:c.2898G=	XP_016865458.1:p.Glu966=
XM_017009970.2:c.2898G=	XP_016865459.1:p.Glu966=
XM_017009971.2:c.2898G=	XP_016865460.1:p.Glu966=
XM_017009974.2:c.2898G=	XP_016865463.1:p.Glu966=
NR_003149.2:n.2997G=