Canonical Allele Identifier: CA2708156393
Gene: ADCY2 HGNC NCBI

Linked Data

dbSNP Id: rs2126527682

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.7517168_7517169del , CM000667.2:g.7517168_7517169del GRCh38
NC_000005.9:g.7517281_7517282del , CM000667.1:g.7517281_7517282del GRCh37
NC_000005.8:g.7570281_7570282del NCBI36
NG_046913.1:g.125939_125940del

Transcript Alleles

HGVS Amino-acid change
ENST00000338316.9:c.409-3570_409-3569del MANE Select ENSP00000342952.4:n.409-3570_409-3569del
ENST00000338316.8:c.409-3570_409-3569del ENSP00000342952.4:n.409-3570_409-3569del
ENST00000484965.5:n.143-3570_143-3569del
ENST00000498598.1:n.108-3570_108-3569del
ENST00000537121.5:c.409-3570_409-3569del ENSP00000444803.2:n.409-3570_409-3569del
NM_020546.2:c.409-3570_409-3569del NP_065433.2:n.409-3570_409-3569del
XM_011513942.1:c.409-3570_409-3569del XP_011512244.1:n.409-3570_409-3569del
XR_427657.2:n.423-3570_423-3569del
XM_011513942.2:c.409-3570_409-3569del XP_011512244.1:n.409-3570_409-3569del
XR_001741973.1:n.423-3570_423-3569del
XR_001741974.2:n.423-3570_423-3569del
NM_020546.3:c.409-3570_409-3569del MANE Select NP_065433.2:n.409-3570_409-3569del