Canonical Allele Identifier: CA813941547
Gene: ADCY2 HGNC NCBI

Linked Data

dbSNP Id: rs1474846251

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.7530594_7530601del , CM000667.2:g.7530594_7530601del GRCh38
NC_000005.9:g.7530707_7530714del , CM000667.1:g.7530707_7530714del GRCh37
NC_000005.8:g.7583707_7583714del NCBI36
NG_046913.1:g.139365_139372del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338316.9:c.570+9695_570+9702del MANE Select ENSP00000342952.4:n.570+9695_570+9702del
ENST00000338316.8:c.570+9695_570+9702del ENSP00000342952.4:n.570+9695_570+9702del
ENST00000498598.1:n.269+9695_269+9702del
ENST00000537121.5:c.565+9695_565+9702del ENSP00000444803.2:n.565+9695_565+9702del
NM_020546.2:c.570+9695_570+9702del NP_065433.2:n.570+9695_570+9702del
XM_011513942.1:c.570+9695_570+9702del XP_011512244.1:n.570+9695_570+9702del
XR_427657.2:n.584+9695_584+9702del
XM_011513942.2:c.570+9695_570+9702del XP_011512244.1:n.570+9695_570+9702del
XR_001741973.1:n.584+9695_584+9702del
XR_001741974.2:n.584+9695_584+9702del
NM_020546.3:c.570+9695_570+9702del MANE Select NP_065433.2:n.570+9695_570+9702del