Canonical Allele Identifier: CA1398327469
Gene: ADCY5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123284670T= , CM000665.2:g.123284670T= GRCh38
NC_000003.11:g.123003517T= , CM000665.1:g.123003517T= GRCh37
NC_000003.10:g.124486207T= NCBI36
NG_033882.1:g.168876A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000466617.6:c.2401A= ENSP00000420082.2:p.Lys801=
ENST00000470367.2:c.2689A= ENSP00000514541.1:p.Lys897=
ENST00000483566.2:c.2401A= ENSP00000420252.2:p.Lys801=
ENST00000699714.1:c.2401A= ENSP00000514539.1:p.Lys801=
ENST00000699715.1:c.2401A= ENSP00000514540.1:p.Lys801=
ENST00000699716.1:c.2401A= ENSP00000514542.1:p.Lys801=
ENST00000699717.1:n.2127A=
ENST00000699718.1:c.3799A= ENSP00000514543.1:p.Lys1267=
ENST00000462833.6:c.3724A= MANE Select ENSP00000419361.1:p.Lys1242=
ENST00000309879.9:c.2674A= ENSP00000308685.5:p.Lys892=
ENST00000462833.5:c.3724A= ENSP00000419361.1:p.Lys1242=
ENST00000478092.1:n.494A=
ENST00000491190.5:c.2698A= ENSP00000418537.1:p.Lys900=
NM_001199642.1:c.2674A= NP_001186571.1:p.Lys892=
NM_183357.2:c.3724A= NP_899200.1:p.Lys1242=
XM_005247077.2:c.3799A= XP_005247134.1:p.Lys1267=
XM_005247078.1:c.2749A= XP_005247135.1:p.Lys917=
XM_006713483.1:c.2698A= XP_006713546.1:p.Lys900=
XM_006713484.1:c.2476A= XP_006713547.1:p.Lys826=
XM_011512359.1:c.2800A= XP_011510661.1:p.Lys934=
XM_011512360.1:c.2710A= XP_011510662.1:p.Lys904=
XM_011512361.1:c.2476A= XP_011510663.1:p.Lys826=
XM_005247077.4:c.3799A= XP_005247134.1:p.Lys1267=
XM_011512359.2:c.2800A= XP_011510661.1:p.Lys934=
XM_011512360.3:c.2710A= XP_011510662.1:p.Lys904=
XM_017005638.1:c.2701A= XP_016861127.1:p.Lys901=
XM_017005639.1:c.2701A= XP_016861128.1:p.Lys901=
NM_001378259.1:c.3799A= NP_001365188.1:p.Lys1267=
NM_183357.3:c.3724A= MANE Select NP_899200.1:p.Lys1242=