Canonical Allele Identifier: CA1562825059

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90617924G= , CM000667.2:g.90617924G=	GRCh38
NC_000005.9:g.89913741G= , CM000667.1:g.89913741G=	GRCh37
NC_000005.8:g.89949497G=	NCBI36
NG_007083.1:g.64125G=
NG_007083.2:g.93581G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.328G= MANE Select	ENSP00000384582.2:p.Glu110=
ENST00000638316.1:n.538G=
ENST00000638638.1:n.735G=
ENST00000640083.1:n.33G=
ENST00000640109.1:n.424G=
ENST00000640281.1:n.387G=
ENST00000405460.6:c.328G=	ENSP00000384582.2:p.Glu110=
ENST00000508842.5:c.340G=	ENSP00000425936.1:p.Glu114=
NM_032119.3:c.328G=	NP_115495.3:p.Glu110=
NR_003149.1:n.424G=
XM_011543675.1:c.328G=	XP_011541977.1:p.Glu110=
XM_011543676.1:c.328G=	XP_011541978.1:p.Glu110=
XM_011543678.1:c.328G=	XP_011541980.1:p.Glu110=
XM_011543679.1:c.328G=	XP_011541981.1:p.Glu110=
NM_032119.4:c.328G= MANE Select	NP_115495.3:p.Glu110=
XM_017009963.2:c.328G=	XP_016865452.1:p.Glu110=
XM_017009964.2:c.328G=	XP_016865453.1:p.Glu110=
XM_017009965.1:c.325G=	XP_016865454.1:p.Glu109=
XM_017009966.2:c.328G=	XP_016865455.1:p.Glu110=
XM_017009967.1:c.328G=	XP_016865456.1:p.Glu110=
XM_017009968.2:c.328G=	XP_016865457.1:p.Glu110=
XM_017009969.2:c.328G=	XP_016865458.1:p.Glu110=
XM_017009970.2:c.328G=	XP_016865459.1:p.Glu110=
XM_017009971.2:c.328G=	XP_016865460.1:p.Glu110=
XM_017009974.2:c.328G=	XP_016865463.1:p.Glu110=
NR_003149.2:n.427G=