Canonical Allele Identifier: CA445416076

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041465C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745648C>A , CM000667.2:g.90745648C>A	GRCh38
NC_000005.9:g.90041465C>A , CM000667.1:g.90041465C>A	GRCh37
NC_000005.8:g.90077221C>A	NCBI36
NG_007083.1:g.191849C>A
NG_007083.2:g.221305C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10827C>A MANE Select	ENSP00000384582.2:p.Ile3609=
ENST00000639431.1:c.265+69439C>A	ENSP00000491057.1:n.265+69439C>A
ENST00000640374.1:n.3971C>A
ENST00000640464.1:n.1246C>A
ENST00000405460.6:c.10827C>A	ENSP00000384582.2:p.Ile3609=
ENST00000509621.1:c.3524C>A
NM_032119.3:c.10827C>A	NP_115495.3:p.Ile3609=
NR_003149.1:n.10840C>A
XM_011543675.1:c.10824C>A	XP_011541977.1:p.Ile3608=
XM_011543676.1:c.10746C>A	XP_011541978.1:p.Ile3582=
XM_011543677.1:c.8130C>A	XP_011541979.1:p.Ile2710=
XM_011543678.1:c.10827C>A	XP_011541980.1:p.Ile3609=
XM_011543679.1:c.*49C>A	XP_011541981.1:n.*49C>A
NM_032119.4:c.10827C>A MANE Select	NP_115495.3:p.Ile3609=
XM_017009963.2:c.10848C>A	XP_016865452.1:p.Ile3616=
XM_017009964.2:c.10845C>A	XP_016865453.1:p.Ile3615=
XM_017009965.1:c.10845C>A	XP_016865454.1:p.Ile3615=
XM_017009966.2:c.10767C>A	XP_016865455.1:p.Ile3589=
XM_017009967.1:c.10752C>A	XP_016865456.1:p.Ile3584=
XM_017009968.2:c.10848C>A	XP_016865457.1:p.Ile3616=
XM_017009969.2:c.10848C>A	XP_016865458.1:p.Ile3616=
XM_017009970.2:c.10848C>A	XP_016865459.1:p.Ile3616=
XM_017009971.2:c.10848C>A	XP_016865460.1:p.Ile3616=
XM_017009972.1:c.3966C>A	XP_016865461.1:p.Ile1322=
XM_017009973.1:c.3945C>A	XP_016865462.1:p.Ile1315=
XM_017009974.2:c.*49C>A	XP_016865463.1:n.*49C>A
NR_003149.2:n.10843C>A