Canonical Allele Identifier: CA1562889758
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90763085_90763086delinsCT , CM000667.2:g.90763085_90763086delinsCT GRCh38
NC_000005.9:g.90058902_90058903delinsCT , CM000667.1:g.90058902_90058903delinsCT GRCh37
NC_000005.8:g.90094658_90094659delinsCT NCBI36
NG_007083.1:g.209286_209287delinsCT
NG_007083.2:g.238742_238743delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.12121-220_12121-219delinsCT MANE Select ENSP00000384582.2:n.12121-220_12121-219delinsCT
ENST00000425867.3:c.1075-220_1075-219delinsCT ENSP00000392618.3:n.1075-220_1075-219delinsCT
ENST00000639431.1:c.265+86876_265+86877delinsCT ENSP00000491057.1:n.265+86876_265+86877delinsCT
ENST00000640464.1:n.2540-220_2540-219delinsCT
ENST00000640729.1:n.478_479delinsCT
ENST00000405460.6:c.12121-220_12121-219delinsCT ENSP00000384582.2:n.12121-220_12121-219delinsCT
NM_032119.3:c.12121-220_12121-219delinsCT NP_115495.3:n.12121-220_12121-219delinsCT
NR_003149.1:n.12134-220_12134-219delinsCT
XM_011543675.1:c.12118-220_12118-219delinsCT XP_011541977.1:n.12118-220_12118-219delinsCT
XM_011543676.1:c.12040-220_12040-219delinsCT XP_011541978.1:n.12040-220_12040-219delinsCT
XM_011543677.1:c.9424-220_9424-219delinsCT XP_011541979.1:n.9424-220_9424-219delinsCT
XM_011543678.1:c.12121-220_12121-219delinsCT XP_011541980.1:n.12121-220_12121-219delinsCT
NM_032119.4:c.12121-220_12121-219delinsCT MANE Select NP_115495.3:n.12121-220_12121-219delinsCT
XM_017009963.2:c.12142-220_12142-219delinsCT XP_016865452.1:n.12142-220_12142-219delinsCT
XM_017009964.2:c.12139-220_12139-219delinsCT XP_016865453.1:n.12139-220_12139-219delinsCT
XM_017009965.1:c.12139-220_12139-219delinsCT XP_016865454.1:n.12139-220_12139-219delinsCT
XM_017009966.2:c.12061-220_12061-219delinsCT XP_016865455.1:n.12061-220_12061-219delinsCT
XM_017009967.1:c.12046-220_12046-219delinsCT XP_016865456.1:n.12046-220_12046-219delinsCT
XM_017009968.2:c.12142-220_12142-219delinsCT XP_016865457.1:n.12142-220_12142-219delinsCT
XM_017009969.2:c.12142-220_12142-219delinsCT XP_016865458.1:n.12142-220_12142-219delinsCT
XM_017009970.2:c.12142-220_12142-219delinsCT XP_016865459.1:n.12142-220_12142-219delinsCT
XM_017009971.2:c.12142-220_12142-219delinsCT XP_016865460.1:n.12142-220_12142-219delinsCT
XM_017009972.1:c.5260-220_5260-219delinsCT XP_016865461.1:n.5260-220_5260-219delinsCT
XM_017009973.1:c.5239-220_5239-219delinsCT XP_016865462.1:n.5239-220_5239-219delinsCT
NR_003149.2:n.12137-220_12137-219delinsCT