Canonical Allele Identifier: CA1562827222

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90622620G= , CM000667.2:g.90622620G=	GRCh38
NC_000005.9:g.89918437G= , CM000667.1:g.89918437G=	GRCh37
NC_000005.8:g.89954193G=	NCBI36
NG_007083.1:g.68821G=
NG_007083.2:g.98277G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.477G= MANE Select	ENSP00000384582.2:p.Glu159=
ENST00000638316.1:n.687G=
ENST00000638638.1:n.884G=
ENST00000640083.1:n.182G=
ENST00000640109.1:n.573G=
ENST00000640281.1:n.536G=
ENST00000405460.6:c.477G=	ENSP00000384582.2:p.Glu159=
ENST00000508842.5:c.393G=	ENSP00000425936.1:p.Glu131=
NM_032119.3:c.477G=	NP_115495.3:p.Glu159=
NR_003149.1:n.573G=
XM_011543675.1:c.477G=	XP_011541977.1:p.Glu159=
XM_011543676.1:c.477G=	XP_011541978.1:p.Glu159=
XM_011543678.1:c.477G=	XP_011541980.1:p.Glu159=
XM_011543679.1:c.477G=	XP_011541981.1:p.Glu159=
NM_032119.4:c.477G= MANE Select	NP_115495.3:p.Glu159=
XM_017009963.2:c.477G=	XP_016865452.1:p.Glu159=
XM_017009964.2:c.477G=	XP_016865453.1:p.Glu159=
XM_017009965.1:c.474G=	XP_016865454.1:p.Glu158=
XM_017009966.2:c.477G=	XP_016865455.1:p.Glu159=
XM_017009967.1:c.381G=	XP_016865456.1:p.Glu127=
XM_017009968.2:c.477G=	XP_016865457.1:p.Glu159=
XM_017009969.2:c.477G=	XP_016865458.1:p.Glu159=
XM_017009970.2:c.477G=	XP_016865459.1:p.Glu159=
XM_017009971.2:c.477G=	XP_016865460.1:p.Glu159=
XM_017009974.2:c.477G=	XP_016865463.1:p.Glu159=
NR_003149.2:n.576G=