Canonical Allele Identifier: CA3339619

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90681364C>A , CM000667.2:g.90681364C>A	GRCh38
NC_000005.9:g.89977181C>A , CM000667.1:g.89977181C>A	GRCh37
NC_000005.8:g.90012937C>A	NCBI36
NG_007083.1:g.127565C>A
NG_007083.2:g.157021C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.5574C>A MANE Select	NP_115495.3:p.Asp1858Glu
ENST00000405460.9:c.5574C>A MANE Select	ENSP00000384582.2:p.Asp1858Glu
NM_032119.3:c.5574C>A	NP_115495.3:p.Asp1858Glu
NR_003149.1:n.5670C>A
NR_003149.2:n.5673C>A
ENST00000405460.6:c.5574C>A	ENSP00000384582.2:p.Asp1858Glu
ENST00000639431.1:c.265+5155C>A	ENSP00000491057.1:n.265+5155C>A
ENST00000639473.1:n.1033C>A
ENST00000640012.1:c.74C>A
ENST00000640403.1:c.2865C>A	ENSP00000492531.1:p.Asp955Glu
ENST00000640779.1:c.386C>A
XM_011543675.1:c.5571C>A	XP_011541977.1:p.Asp1857Glu
XM_011543676.1:c.5493C>A	XP_011541978.1:p.Asp1831Glu
XM_011543677.1:c.2877C>A	XP_011541979.1:p.Asp959Glu
XM_011543678.1:c.5574C>A	XP_011541980.1:p.Asp1858Glu
XM_011543679.1:c.5574C>A	XP_011541981.1:p.Asp1858Glu
XM_017009963.2:c.5574C>A	XP_016865452.1:p.Asp1858Glu
XM_017009964.2:c.5571C>A	XP_016865453.1:p.Asp1857Glu
XM_017009965.1:c.5571C>A	XP_016865454.1:p.Asp1857Glu
XM_017009966.2:c.5493C>A	XP_016865455.1:p.Asp1831Glu
XM_017009967.1:c.5478C>A	XP_016865456.1:p.Asp1826Glu
XM_017009968.2:c.5574C>A	XP_016865457.1:p.Asp1858Glu
XM_017009969.2:c.5574C>A	XP_016865458.1:p.Asp1858Glu
XM_017009970.2:c.5574C>A	XP_016865459.1:p.Asp1858Glu
XM_017009971.2:c.5574C>A	XP_016865460.1:p.Asp1858Glu
XM_017009973.1:c.-1226C>A	XP_016865462.1:n.-1226C>A
XM_017009974.2:c.5574C>A	XP_016865463.1:p.Asp1858Glu