Canonical Allele Identifier: CA1398346236
Gene: ADCY5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123325349G= , CM000665.2:g.123325349G= GRCh38
NC_000003.11:g.123044196G= , CM000665.1:g.123044196G= GRCh37
NC_000003.10:g.124526886G= NCBI36
NG_033882.1:g.128197C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000466617.6:c.738C= ENSP00000420082.2:p.Asn246=
ENST00000470367.2:c.1026C= ENSP00000514541.1:p.Asn342=
ENST00000483566.2:c.738C= ENSP00000420252.2:p.Asn246=
ENST00000699714.1:c.738C= ENSP00000514539.1:p.Asn246=
ENST00000699715.1:c.738C= ENSP00000514540.1:p.Asn246=
ENST00000699716.1:c.738C= ENSP00000514542.1:p.Asn246=
ENST00000699718.1:c.2061C= ENSP00000514543.1:p.Asn687=
ENST00000699719.1:n.320C=
ENST00000462833.6:c.2061C= MANE Select ENSP00000419361.1:p.Asn687=
ENST00000309879.9:c.1011C= ENSP00000308685.5:p.Asn337=
ENST00000462833.5:c.2061C= ENSP00000419361.1:p.Asn687=
ENST00000466617.5:c.738C= ENSP00000420082.1:p.Asn246=
ENST00000491190.5:c.960C= ENSP00000418537.1:p.Asn320=
NM_001199642.1:c.1011C= NP_001186571.1:p.Asn337=
NM_183357.2:c.2061C= NP_899200.1:p.Asn687=
XM_005247077.2:c.2061C= XP_005247134.1:p.Asn687=
XM_005247078.1:c.1011C= XP_005247135.1:p.Asn337=
XM_006713483.1:c.960C= XP_006713546.1:p.Asn320=
XM_006713484.1:c.738C= XP_006713547.1:p.Asn246=
XM_011512358.1:c.2061C= XP_011510660.1:p.Asn687=
XM_011512359.1:c.1062C= XP_011510661.1:p.Asn354=
XM_011512360.1:c.972C= XP_011510662.1:p.Asn324=
XM_011512361.1:c.738C= XP_011510663.1:p.Asn246=
XM_005247077.4:c.2061C= XP_005247134.1:p.Asn687=
XM_011512359.2:c.1062C= XP_011510661.1:p.Asn354=
XM_011512360.3:c.972C= XP_011510662.1:p.Asn324=
XM_017005638.1:c.963C= XP_016861127.1:p.Asn321=
XM_017005639.1:c.963C= XP_016861128.1:p.Asn321=
NM_001378259.1:c.2061C= NP_001365188.1:p.Asn687=
NM_183357.3:c.2061C= MANE Select NP_899200.1:p.Asn687=