Canonical Allele Identifier: CA354223368
Gene: ADCY5 HGNC NCBI

Linked Data

dbSNP Id: rs1553717575

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123291136C>A , CM000665.2:g.123291136C>A GRCh38
NC_000003.11:g.123009983C>A , CM000665.1:g.123009983C>A GRCh37
NC_000003.10:g.124492673C>A NCBI36
NG_033882.1:g.162410G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000466617.6:c.1981G>T ENSP00000420082.2:p.Glu661Ter
ENST00000470367.2:c.2269G>T ENSP00000514541.1:p.Glu757Ter
ENST00000483566.2:c.1981G>T ENSP00000420252.2:p.Glu661Ter
ENST00000699714.1:c.1981G>T ENSP00000514539.1:p.Glu661Ter
ENST00000699715.1:c.1981G>T ENSP00000514540.1:p.Glu661Ter
ENST00000699716.1:c.1981G>T ENSP00000514542.1:p.Glu661Ter
ENST00000699717.1:n.1707G>T
ENST00000699718.1:c.3379G>T ENSP00000514543.1:p.Glu1127Ter
ENST00000462833.6:c.3304G>T MANE Select ENSP00000419361.1:p.Glu1102Ter
ENST00000309879.9:c.2254G>T ENSP00000308685.5:p.Glu752Ter
ENST00000462833.5:c.3304G>T ENSP00000419361.1:p.Glu1102Ter
ENST00000491190.5:c.2278G>T ENSP00000418537.1:p.Glu760Ter
NM_001199642.1:c.2254G>T NP_001186571.1:p.Glu752Ter
NM_183357.2:c.3304G>T NP_899200.1:p.Glu1102Ter
XM_005247077.2:c.3379G>T XP_005247134.1:p.Glu1127Ter
XM_005247078.1:c.2329G>T XP_005247135.1:p.Glu777Ter
XM_006713483.1:c.2278G>T XP_006713546.1:p.Glu760Ter
XM_006713484.1:c.2056G>T XP_006713547.1:p.Glu686Ter
XM_011512359.1:c.2380G>T XP_011510661.1:p.Glu794Ter
XM_011512360.1:c.2290G>T XP_011510662.1:p.Glu764Ter
XM_011512361.1:c.2056G>T XP_011510663.1:p.Glu686Ter
XM_005247077.4:c.3379G>T XP_005247134.1:p.Glu1127Ter
XM_011512359.2:c.2380G>T XP_011510661.1:p.Glu794Ter
XM_011512360.3:c.2290G>T XP_011510662.1:p.Glu764Ter
XM_017005638.1:c.2281G>T XP_016861127.1:p.Glu761Ter
XM_017005639.1:c.2281G>T XP_016861128.1:p.Glu761Ter
NM_001378259.1:c.3379G>T NP_001365188.1:p.Glu1127Ter
NM_183357.3:c.3304G>T MANE Select NP_899200.1:p.Glu1102Ter