Canonical Allele Identifier: CA1398343583
Gene: ADCY5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123319805T= , CM000665.2:g.123319805T= GRCh38
NC_000003.11:g.123038652T= , CM000665.1:g.123038652T= GRCh37
NC_000003.10:g.124521342T= NCBI36
NG_033882.1:g.133741A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000466617.6:c.802A= ENSP00000420082.2:p.Ser268=
ENST00000470367.2:c.1090A= ENSP00000514541.1:p.Ser364=
ENST00000483566.2:c.802A= ENSP00000420252.2:p.Ser268=
ENST00000699714.1:c.802A= ENSP00000514539.1:p.Ser268=
ENST00000699715.1:c.802A= ENSP00000514540.1:p.Ser268=
ENST00000699716.1:c.802A= ENSP00000514542.1:p.Ser268=
ENST00000699718.1:c.2125A= ENSP00000514543.1:p.Ser709=
ENST00000699719.1:n.384A=
ENST00000462833.6:c.2125A= MANE Select ENSP00000419361.1:p.Ser709=
ENST00000309879.9:c.1075A= ENSP00000308685.5:p.Ser359=
ENST00000462833.5:c.2125A= ENSP00000419361.1:p.Ser709=
ENST00000466617.5:c.802A= ENSP00000420082.1:p.Ser268=
ENST00000491190.5:c.1024A= ENSP00000418537.1:p.Ser342=
NM_001199642.1:c.1075A= NP_001186571.1:p.Ser359=
NM_183357.2:c.2125A= NP_899200.1:p.Ser709=
XM_005247077.2:c.2125A= XP_005247134.1:p.Ser709=
XM_005247078.1:c.1075A= XP_005247135.1:p.Ser359=
XM_006713483.1:c.1024A= XP_006713546.1:p.Ser342=
XM_006713484.1:c.802A= XP_006713547.1:p.Ser268=
XM_011512358.1:c.2125A= XP_011510660.1:p.Ser709=
XM_011512359.1:c.1126A= XP_011510661.1:p.Ser376=
XM_011512360.1:c.1036A= XP_011510662.1:p.Ser346=
XM_011512361.1:c.802A= XP_011510663.1:p.Ser268=
XM_005247077.4:c.2125A= XP_005247134.1:p.Ser709=
XM_011512359.2:c.1126A= XP_011510661.1:p.Ser376=
XM_011512360.3:c.1036A= XP_011510662.1:p.Ser346=
XM_017005638.1:c.1027A= XP_016861127.1:p.Ser343=
XM_017005639.1:c.1027A= XP_016861128.1:p.Ser343=
NM_001378259.1:c.2125A= NP_001365188.1:p.Ser709=
NM_183357.3:c.2125A= MANE Select NP_899200.1:p.Ser709=