Canonical Allele Identifier: CA1525647191
Gene: ADCY2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.7530644_7530645delinsCT , CM000667.2:g.7530644_7530645delinsCT GRCh38
NC_000005.9:g.7530757_7530758delinsCT , CM000667.1:g.7530757_7530758delinsCT GRCh37
NC_000005.8:g.7583757_7583758delinsCT NCBI36
NG_046913.1:g.139415_139416delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000338316.9:c.570+9745_570+9746delinsCT MANE Select ENSP00000342952.4:n.570+9745_570+9746deli...
ENST00000338316.8:c.570+9745_570+9746delinsCT ENSP00000342952.4:n.570+9745_570+9746deli...
ENST00000498598.1:n.269+9745_269+9746delinsCT
ENST00000537121.5:c.565+9745_565+9746delinsCT ENSP00000444803.2:n.565+9745_565+9746deli...
NM_020546.2:c.570+9745_570+9746delinsCT NP_065433.2:n.570+9745_570+9746delinsCT
XM_011513942.1:c.570+9745_570+9746delinsCT XP_011512244.1:n.570+9745_570+9746delinsC...
XR_427657.2:n.584+9745_584+9746delinsCT
XM_011513942.2:c.570+9745_570+9746delinsCT XP_011512244.1:n.570+9745_570+9746delinsC...
XR_001741973.1:n.584+9745_584+9746delinsCT
XR_001741974.2:n.584+9745_584+9746delinsCT
NM_020546.3:c.570+9745_570+9746delinsCT MANE Select NP_065433.2:n.570+9745_570+9746delinsCT