Canonical Allele Identifier: CA1398358745
Gene: ADCY5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123352444C= , CM000665.2:g.123352444C= GRCh38
NC_000003.11:g.123071291C= , CM000665.1:g.123071291C= GRCh37
NC_000003.10:g.124553981C= NCBI36
NG_033882.1:g.101102G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000466617.6:c.-52G= ENSP00000420082.2:n.-52G=
ENST00000470367.2:c.237G= ENSP00000514541.1:p.Glu79=
ENST00000483566.2:c.-52G= ENSP00000420252.2:n.-52G=
ENST00000699714.1:c.-52G= ENSP00000514539.1:n.-52G=
ENST00000699715.1:c.-52G= ENSP00000514540.1:n.-52G=
ENST00000699716.1:c.-52G= ENSP00000514542.1:n.-52G=
ENST00000699718.1:c.1272G= ENSP00000514543.1:p.Glu424=
ENST00000462833.6:c.1272G= MANE Select ENSP00000419361.1:p.Glu424=
ENST00000309879.9:c.222G= ENSP00000308685.5:p.Glu74=
ENST00000462833.5:c.1272G= ENSP00000419361.1:p.Glu424=
ENST00000466617.5:c.-52G= ENSP00000420082.1:n.-52G=
ENST00000476455.1:c.176G= ENSP00000417789.1:p.Arg59=
ENST00000483566.1:c.-52G= ENSP00000420252.1:n.-52G=
ENST00000491190.5:c.171G= ENSP00000418537.1:p.Glu57=
NM_001199642.1:c.222G= NP_001186571.1:p.Glu74=
NM_183357.2:c.1272G= NP_899200.1:p.Glu424=
XM_005247077.2:c.1272G= XP_005247134.1:p.Glu424=
XM_005247078.1:c.222G= XP_005247135.1:p.Glu74=
XM_006713483.1:c.171G= XP_006713546.1:p.Glu57=
XM_006713484.1:c.-52G= XP_006713547.1:n.-52G=
XM_011512358.1:c.1272G= XP_011510660.1:p.Glu424=
XM_011512359.1:c.273G= XP_011510661.1:p.Glu91=
XM_011512360.1:c.183G= XP_011510662.1:p.Glu61=
XM_011512361.1:c.-52G= XP_011510663.1:n.-52G=
XM_005247077.4:c.1272G= XP_005247134.1:p.Glu424=
XM_011512359.2:c.273G= XP_011510661.1:p.Glu91=
XM_011512360.3:c.183G= XP_011510662.1:p.Glu61=
XM_017005638.1:c.174G= XP_016861127.1:p.Glu58=
XM_017005639.1:c.174G= XP_016861128.1:p.Glu58=
NM_001378259.1:c.1272G= NP_001365188.1:p.Glu424=
NM_183357.3:c.1272G= MANE Select NP_899200.1:p.Glu424=