Canonical Allele Identifier: CA360366519
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90755043C>A , CM000667.2:g.90755043C>A GRCh38
NC_000005.9:g.90050860C>A , CM000667.1:g.90050860C>A GRCh37
NC_000005.8:g.90086616C>A NCBI36
NG_007083.1:g.201244C>A
NG_007083.2:g.230700C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.11438C>A MANE Select ENSP00000384582.2:p.Ala3813Asp
ENST00000425867.3:c.569C>A ENSP00000392618.3:p.Ala190Asp
ENST00000639431.1:c.265+78834C>A ENSP00000491057.1:n.265+78834C>A
ENST00000640374.1:n.4582C>A
ENST00000640464.1:n.1857C>A
ENST00000405460.6:c.11438C>A ENSP00000384582.2:p.Ala3813Asp
ENST00000509621.1:c.4135C>A
NM_032119.3:c.11438C>A NP_115495.3:p.Ala3813Asp
NR_003149.1:n.11451C>A
XM_011543675.1:c.11435C>A XP_011541977.1:p.Ala3812Asp
XM_011543676.1:c.11357C>A XP_011541978.1:p.Ala3786Asp
XM_011543677.1:c.8741C>A XP_011541979.1:p.Ala2914Asp
XM_011543678.1:c.11438C>A XP_011541980.1:p.Ala3813Asp
NM_032119.4:c.11438C>A MANE Select NP_115495.3:p.Ala3813Asp
XM_017009963.2:c.11459C>A XP_016865452.1:p.Ala3820Asp
XM_017009964.2:c.11456C>A XP_016865453.1:p.Ala3819Asp
XM_017009965.1:c.11456C>A XP_016865454.1:p.Ala3819Asp
XM_017009966.2:c.11378C>A XP_016865455.1:p.Ala3793Asp
XM_017009967.1:c.11363C>A XP_016865456.1:p.Ala3788Asp
XM_017009968.2:c.11459C>A XP_016865457.1:p.Ala3820Asp
XM_017009969.2:c.11459C>A XP_016865458.1:p.Ala3820Asp
XM_017009970.2:c.11459C>A XP_016865459.1:p.Ala3820Asp
XM_017009971.2:c.11459C>A XP_016865460.1:p.Ala3820Asp
XM_017009972.1:c.4577C>A XP_016865461.1:p.Ala1526Asp
XM_017009973.1:c.4556C>A XP_016865462.1:p.Ala1519Asp
NR_003149.2:n.11454C>A