Canonical Allele Identifier: CA1398330457
Gene: ADCY5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123291364T= , CM000665.2:g.123291364T= GRCh38
NC_000003.11:g.123010211T= , CM000665.1:g.123010211T= GRCh37
NC_000003.10:g.124492901T= NCBI36
NG_033882.1:g.162182A=

Transcript Alleles

HGVS Amino-acid change
ENST00000466617.6:c.1753A= ENSP00000420082.2:p.Lys585=
ENST00000470367.2:c.2041A= ENSP00000514541.1:p.Lys681=
ENST00000483566.2:c.1753A= ENSP00000420252.2:p.Lys585=
ENST00000699714.1:c.1753A= ENSP00000514539.1:p.Lys585=
ENST00000699715.1:c.1753A= ENSP00000514540.1:p.Lys585=
ENST00000699716.1:c.1753A= ENSP00000514542.1:p.Lys585=
ENST00000699717.1:n.1479A=
ENST00000699718.1:c.3151A= ENSP00000514543.1:p.Lys1051=
ENST00000462833.6:c.3076A= MANE Select ENSP00000419361.1:p.Lys1026=
ENST00000309879.9:c.2026A= ENSP00000308685.5:p.Lys676=
ENST00000462833.5:c.3076A= ENSP00000419361.1:p.Lys1026=
ENST00000491190.5:c.2050A= ENSP00000418537.1:p.Lys684=
NM_001199642.1:c.2026A= NP_001186571.1:p.Lys676=
NM_183357.2:c.3076A= NP_899200.1:p.Lys1026=
XM_005247077.2:c.3151A= XP_005247134.1:p.Lys1051=
XM_005247078.1:c.2101A= XP_005247135.1:p.Lys701=
XM_006713483.1:c.2050A= XP_006713546.1:p.Lys684=
XM_006713484.1:c.1828A= XP_006713547.1:p.Lys610=
XM_011512359.1:c.2152A= XP_011510661.1:p.Lys718=
XM_011512360.1:c.2062A= XP_011510662.1:p.Lys688=
XM_011512361.1:c.1828A= XP_011510663.1:p.Lys610=
XM_005247077.4:c.3151A= XP_005247134.1:p.Lys1051=
XM_011512359.2:c.2152A= XP_011510661.1:p.Lys718=
XM_011512360.3:c.2062A= XP_011510662.1:p.Lys688=
XM_017005638.1:c.2053A= XP_016861127.1:p.Lys685=
XM_017005639.1:c.2053A= XP_016861128.1:p.Lys685=
NM_001378259.1:c.3151A= NP_001365188.1:p.Lys1051=
NM_183357.3:c.3076A= MANE Select NP_899200.1:p.Lys1026=