Canonical Allele Identifier: CA2767415133

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90617930_90617932del , CM000667.2:g.90617930_90617932del	GRCh38
NC_000005.9:g.89913747_89913749del , CM000667.1:g.89913747_89913749del	GRCh37
NC_000005.8:g.89949503_89949505del	NCBI36
NG_007083.1:g.64131_64133del
NG_007083.2:g.93587_93589del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.334_336del MANE Select	ENSP00000384582.2:p.Phe112del
ENST00000638316.1:n.544_546del
ENST00000638638.1:n.741_743del
ENST00000640083.1:n.39_41del
ENST00000640109.1:n.430_432del
ENST00000640281.1:n.393_395del
ENST00000405460.6:c.334_336del	ENSP00000384582.2:p.Phe112del
ENST00000508842.5:c.346_348del	ENSP00000425936.1:p.Phe116del
NM_032119.3:c.334_336del	NP_115495.3:p.Phe112del
NR_003149.1:n.430_432del
XM_011543675.1:c.334_336del	XP_011541977.1:p.Phe112del
XM_011543676.1:c.334_336del	XP_011541978.1:p.Phe112del
XM_011543678.1:c.334_336del	XP_011541980.1:p.Phe112del
XM_011543679.1:c.334_336del	XP_011541981.1:p.Phe112del
NM_032119.4:c.334_336del MANE Select	NP_115495.3:p.Phe112del
XM_017009963.2:c.334_336del	XP_016865452.1:p.Phe112del
XM_017009964.2:c.334_336del	XP_016865453.1:p.Phe112del
XM_017009965.1:c.331_333del	XP_016865454.1:p.Phe111del
XM_017009966.2:c.334_336del	XP_016865455.1:p.Phe112del
XM_017009967.1:c.334_336del	XP_016865456.1:p.Phe112del
XM_017009968.2:c.334_336del	XP_016865457.1:p.Phe112del
XM_017009969.2:c.334_336del	XP_016865458.1:p.Phe112del
XM_017009970.2:c.334_336del	XP_016865459.1:p.Phe112del
XM_017009971.2:c.334_336del	XP_016865460.1:p.Phe112del
XM_017009974.2:c.334_336del	XP_016865463.1:p.Phe112del
NR_003149.2:n.433_435del