Canonical Allele Identifier: CA1398327360
Gene: ADCY5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123284482A= , CM000665.2:g.123284482A= GRCh38
NC_000003.11:g.123003329A= , CM000665.1:g.123003329A= GRCh37
NC_000003.10:g.124486019A= NCBI36
NG_033882.1:g.169064T=

Transcript Alleles

HGVS Amino-acid change
ENST00000466617.6:c.*126T= ENSP00000420082.2:n.*126T=
ENST00000470367.2:c.*126T= ENSP00000514541.1:n.*126T=
ENST00000483566.2:c.*126T= ENSP00000420252.2:n.*126T=
ENST00000699714.1:c.*126T= ENSP00000514539.1:n.*126T=
ENST00000699715.1:c.*126T= ENSP00000514540.1:n.*126T=
ENST00000699716.1:c.*126T= ENSP00000514542.1:n.*126T=
ENST00000699717.1:n.2315T=
ENST00000699718.1:c.3987T= ENSP00000514543.1:n.3987T=
ENST00000462833.6:c.*126T= MANE Select ENSP00000419361.1:n.*126T=
ENST00000462833.5:c.*126T= ENSP00000419361.1:n.*126T=
ENST00000478092.1:n.682T=
ENST00000491190.5:c.*126T= ENSP00000418537.1:n.*126T=
NM_001199642.1:c.*126T= NP_001186571.1:n.*126T=
NM_183357.2:c.3912T= NP_899200.1:n.3912T=
XM_005247077.2:c.*126T= XP_005247134.1:n.*126T=
XM_005247078.1:c.*126T= XP_005247135.1:n.*126T=
XM_006713483.1:c.*126T= XP_006713546.1:n.*126T=
XM_006713484.1:c.*126T= XP_006713547.1:n.*126T=
XM_011512359.1:c.*126T= XP_011510661.1:n.*126T=
XM_011512360.1:c.*126T= XP_011510662.1:n.*126T=
XM_011512361.1:c.*126T= XP_011510663.1:n.*126T=
XM_005247077.4:c.*126T= XP_005247134.1:n.*126T=
XM_011512359.2:c.*126T= XP_011510661.1:n.*126T=
XM_011512360.3:c.*126T= XP_011510662.1:n.*126T=
XM_017005638.1:c.*126T= XP_016861127.1:n.*126T=
XM_017005639.1:c.*126T= XP_016861128.1:n.*126T=
NM_001378259.1:c.*126T= NP_001365188.1:n.*126T=
NM_183357.3:c.*126T= MANE Select NP_899200.1:n.*126T=