Canonical Allele Identifier: CA2767424511
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90823626_90823627insGT , CM000667.2:g.90823626_90823627insGT GRCh38
NC_000005.9:g.90119443_90119444insGT , CM000667.1:g.90119443_90119444insGT GRCh37
NC_000005.8:g.90155199_90155200insGT NCBI36
NG_007083.1:g.269827_269828insGT
NG_007083.2:g.299283_299284insGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.16368+30_16368+31insGT MANE Select ENSP00000384582.2:n.16368+30_16368+31insGT
ENST00000425867.3:c.5322+30_5322+31insGT ENSP00000392618.3:n.5322+30_5322+31insGT
ENST00000638510.1:n.3635+30_3635+31insGT
ENST00000639431.1:c.265+147417_265+147418insGT ENSP00000491057.1:n.265+147417_265+147418insGT
ENST00000640061.1:n.128+1444_128+1445insGT
ENST00000640407.1:c.2778+30_2778+31insGT ENSP00000491425.1:n.2778+30_2778+31insGT
ENST00000405460.6:c.16368+30_16368+31insGT ENSP00000384582.2:n.16368+30_16368+31insGT
ENST00000425867.2:c.3351+30_3351+31insGT ENSP00000392618.2:n.3351+30_3351+31insGT
NM_032119.3:c.16368+30_16368+31insGT NP_115495.3:n.16368+30_16368+31insGT
NR_003149.1:n.16381+30_16381+31insGT
XM_011543675.1:c.16365+30_16365+31insGT XP_011541977.1:n.16365+30_16365+31insGT
XM_011543676.1:c.16287+30_16287+31insGT XP_011541978.1:n.16287+30_16287+31insGT
XM_011543677.1:c.13671+30_13671+31insGT XP_011541979.1:n.13671+30_13671+31insGT
NM_032119.4:c.16368+30_16368+31insGT MANE Select NP_115495.3:n.16368+30_16368+31insGT
XM_017009963.2:c.16389+30_16389+31insGT XP_016865452.1:n.16389+30_16389+31insGT
XM_017009964.2:c.16386+30_16386+31insGT XP_016865453.1:n.16386+30_16386+31insGT
XM_017009965.1:c.16386+30_16386+31insGT XP_016865454.1:n.16386+30_16386+31insGT
XM_017009966.2:c.16308+30_16308+31insGT XP_016865455.1:n.16308+30_16308+31insGT
XM_017009967.1:c.16293+30_16293+31insGT XP_016865456.1:n.16293+30_16293+31insGT
XM_017009968.2:c.16209+30_16209+31insGT XP_016865457.1:n.16209+30_16209+31insGT
XM_017009969.2:c.16389+30_16389+31insGT XP_016865458.1:n.16389+30_16389+31insGT
XM_017009972.1:c.9507+30_9507+31insGT XP_016865461.1:n.9507+30_9507+31insGT
XM_017009973.1:c.9486+30_9486+31insGT XP_016865462.1:n.9486+30_9486+31insGT
NR_003149.2:n.16384+30_16384+31insGT