Canonical Allele Identifier: CA813935694
Gene: ADCY2 HGNC NCBI

Linked Data

dbSNP Id: rs1436582803

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.7517229_7517239del , CM000667.2:g.7517229_7517239del GRCh38
NC_000005.9:g.7517342_7517352del , CM000667.1:g.7517342_7517352del GRCh37
NC_000005.8:g.7570342_7570352del NCBI36
NG_046913.1:g.126000_126010del

Transcript Alleles

HGVS Amino-acid change
ENST00000338316.9:c.409-3509_409-3499del MANE Select ENSP00000342952.4:n.409-3509_409-3499del
ENST00000338316.8:c.409-3509_409-3499del ENSP00000342952.4:n.409-3509_409-3499del
ENST00000484965.5:n.143-3509_143-3499del
ENST00000498598.1:n.108-3509_108-3499del
ENST00000537121.5:c.409-3509_409-3499del ENSP00000444803.2:n.409-3509_409-3499del
NM_020546.2:c.409-3509_409-3499del NP_065433.2:n.409-3509_409-3499del
XM_011513942.1:c.409-3509_409-3499del XP_011512244.1:n.409-3509_409-3499del
XR_427657.2:n.423-3509_423-3499del
XM_011513942.2:c.409-3509_409-3499del XP_011512244.1:n.409-3509_409-3499del
XR_001741973.1:n.423-3509_423-3499del
XR_001741974.2:n.423-3509_423-3499del
NM_020546.3:c.409-3509_409-3499del MANE Select NP_065433.2:n.409-3509_409-3499del