Canonical Allele Identifier: CA1562867522

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712300C= , CM000667.2:g.90712300C=	GRCh38
NC_000005.9:g.90008117C= , CM000667.1:g.90008117C=	GRCh37
NC_000005.8:g.90043873C=	NCBI36
NG_007083.1:g.158501C=
NG_007083.2:g.187957C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9056C= MANE Select	ENSP00000384582.2:p.Ala3019=
ENST00000639431.1:c.265+36091C=	ENSP00000491057.1:n.265+36091C=
ENST00000639473.1:n.4515C=
ENST00000640012.1:c.2863C=
ENST00000640374.1:n.2200C=
ENST00000640779.1:c.3785C=
ENST00000405460.6:c.9056C=	ENSP00000384582.2:p.Ala3019=
ENST00000509621.1:c.1753C=
NM_032119.3:c.9056C=	NP_115495.3:p.Ala3019=
NR_003149.1:n.9069C=
XM_011543675.1:c.9053C=	XP_011541977.1:p.Ala3018=
XM_011543676.1:c.8975C=	XP_011541978.1:p.Ala2992=
XM_011543677.1:c.6359C=	XP_011541979.1:p.Ala2120=
XM_011543678.1:c.9056C=	XP_011541980.1:p.Ala3019=
XM_011543679.1:c.9056C=	XP_011541981.1:p.Ala3019=
NM_032119.4:c.9056C= MANE Select	NP_115495.3:p.Ala3019=
XM_017009963.2:c.9077C=	XP_016865452.1:p.Ala3026=
XM_017009964.2:c.9074C=	XP_016865453.1:p.Ala3025=
XM_017009965.1:c.9074C=	XP_016865454.1:p.Ala3025=
XM_017009966.2:c.8996C=	XP_016865455.1:p.Ala2999=
XM_017009967.1:c.8981C=	XP_016865456.1:p.Ala2994=
XM_017009968.2:c.9077C=	XP_016865457.1:p.Ala3026=
XM_017009969.2:c.9077C=	XP_016865458.1:p.Ala3026=
XM_017009970.2:c.9077C=	XP_016865459.1:p.Ala3026=
XM_017009971.2:c.9077C=	XP_016865460.1:p.Ala3026=
XM_017009972.1:c.2195C=	XP_016865461.1:p.Ala732=
XM_017009973.1:c.2174C=	XP_016865462.1:p.Ala725=
XM_017009974.2:c.9077C=	XP_016865463.1:p.Ala3026=
NR_003149.2:n.9072C=