Canonical Allele Identifier: CA1398343574
Gene: ADCY5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123319781C= , CM000665.2:g.123319781C= GRCh38
NC_000003.11:g.123038628C= , CM000665.1:g.123038628C= GRCh37
NC_000003.10:g.124521318C= NCBI36
NG_033882.1:g.133765G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000466617.6:c.826G= ENSP00000420082.2:p.Asp276=
ENST00000470367.2:c.1114G= ENSP00000514541.1:p.Asp372=
ENST00000483566.2:c.826G= ENSP00000420252.2:p.Asp276=
ENST00000699714.1:c.826G= ENSP00000514539.1:p.Asp276=
ENST00000699715.1:c.826G= ENSP00000514540.1:p.Asp276=
ENST00000699716.1:c.826G= ENSP00000514542.1:p.Asp276=
ENST00000699718.1:c.2149G= ENSP00000514543.1:p.Asp717=
ENST00000699719.1:n.408G=
ENST00000462833.6:c.2149G= MANE Select ENSP00000419361.1:p.Asp717=
ENST00000309879.9:c.1099G= ENSP00000308685.5:p.Asp367=
ENST00000462833.5:c.2149G= ENSP00000419361.1:p.Asp717=
ENST00000466617.5:c.826G= ENSP00000420082.1:p.Asp276=
ENST00000491190.5:c.1048G= ENSP00000418537.1:p.Asp350=
NM_001199642.1:c.1099G= NP_001186571.1:p.Asp367=
NM_183357.2:c.2149G= NP_899200.1:p.Asp717=
XM_005247077.2:c.2149G= XP_005247134.1:p.Asp717=
XM_005247078.1:c.1099G= XP_005247135.1:p.Asp367=
XM_006713483.1:c.1048G= XP_006713546.1:p.Asp350=
XM_006713484.1:c.826G= XP_006713547.1:p.Asp276=
XM_011512358.1:c.2149G= XP_011510660.1:p.Asp717=
XM_011512359.1:c.1150G= XP_011510661.1:p.Asp384=
XM_011512360.1:c.1060G= XP_011510662.1:p.Asp354=
XM_011512361.1:c.826G= XP_011510663.1:p.Asp276=
XM_005247077.4:c.2149G= XP_005247134.1:p.Asp717=
XM_011512359.2:c.1150G= XP_011510661.1:p.Asp384=
XM_011512360.3:c.1060G= XP_011510662.1:p.Asp354=
XM_017005638.1:c.1051G= XP_016861127.1:p.Asp351=
XM_017005639.1:c.1051G= XP_016861128.1:p.Asp351=
NM_001378259.1:c.2149G= NP_001365188.1:p.Asp717=
NM_183357.3:c.2149G= MANE Select NP_899200.1:p.Asp717=