Canonical Allele Identifier: CA1398327441
Gene: ADCY5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123284615A= , CM000665.2:g.123284615A= GRCh38
NC_000003.11:g.123003462A= , CM000665.1:g.123003462A= GRCh37
NC_000003.10:g.124486152A= NCBI36
NG_033882.1:g.168931T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000466617.6:c.2456T= ENSP00000420082.2:p.Leu819=
ENST00000470367.2:c.2744T= ENSP00000514541.1:p.Leu915=
ENST00000483566.2:c.2456T= ENSP00000420252.2:p.Leu819=
ENST00000699714.1:c.2456T= ENSP00000514539.1:p.Leu819=
ENST00000699715.1:c.2456T= ENSP00000514540.1:p.Leu819=
ENST00000699716.1:c.2456T= ENSP00000514542.1:p.Leu819=
ENST00000699717.1:n.2182T=
ENST00000699718.1:c.3854T= ENSP00000514543.1:p.Leu1285=
ENST00000462833.6:c.3779T= MANE Select ENSP00000419361.1:p.Leu1260=
ENST00000309879.9:c.2729T= ENSP00000308685.5:p.Leu910=
ENST00000462833.5:c.3779T= ENSP00000419361.1:p.Leu1260=
ENST00000478092.1:n.549T=
ENST00000491190.5:c.2753T= ENSP00000418537.1:p.Leu918=
NM_001199642.1:c.2729T= NP_001186571.1:p.Leu910=
NM_183357.2:c.3779T= NP_899200.1:p.Leu1260=
XM_005247077.2:c.3854T= XP_005247134.1:p.Leu1285=
XM_005247078.1:c.2804T= XP_005247135.1:p.Leu935=
XM_006713483.1:c.2753T= XP_006713546.1:p.Leu918=
XM_006713484.1:c.2531T= XP_006713547.1:p.Leu844=
XM_011512359.1:c.2855T= XP_011510661.1:p.Leu952=
XM_011512360.1:c.2765T= XP_011510662.1:p.Leu922=
XM_011512361.1:c.2531T= XP_011510663.1:p.Leu844=
XM_005247077.4:c.3854T= XP_005247134.1:p.Leu1285=
XM_011512359.2:c.2855T= XP_011510661.1:p.Leu952=
XM_011512360.3:c.2765T= XP_011510662.1:p.Leu922=
XM_017005638.1:c.2756T= XP_016861127.1:p.Leu919=
XM_017005639.1:c.2756T= XP_016861128.1:p.Leu919=
NM_001378259.1:c.3854T= NP_001365188.1:p.Leu1285=
NM_183357.3:c.3779T= MANE Select NP_899200.1:p.Leu1260=