Canonical Allele Identifier: CA354218299
Gene: ADCY5 HGNC NCBI

Linked Data

dbSNP Id: rs1348727791

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123325335T>C , CM000665.2:g.123325335T>C GRCh38
NC_000003.11:g.123044182T>C , CM000665.1:g.123044182T>C GRCh37
NC_000003.10:g.124526872T>C NCBI36
NG_033882.1:g.128211A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000466617.6:c.752A>G ENSP00000420082.2:p.Glu251Gly
ENST00000470367.2:c.1040A>G ENSP00000514541.1:p.Glu347Gly
ENST00000483566.2:c.752A>G ENSP00000420252.2:p.Glu251Gly
ENST00000699714.1:c.752A>G ENSP00000514539.1:p.Glu251Gly
ENST00000699715.1:c.752A>G ENSP00000514540.1:p.Glu251Gly
ENST00000699716.1:c.752A>G ENSP00000514542.1:p.Glu251Gly
ENST00000699718.1:c.2075A>G ENSP00000514543.1:p.Glu692Gly
ENST00000699719.1:n.334A>G
ENST00000462833.6:c.2075A>G MANE Select ENSP00000419361.1:p.Glu692Gly
ENST00000309879.9:c.1025A>G ENSP00000308685.5:p.Glu342Gly
ENST00000462833.5:c.2075A>G ENSP00000419361.1:p.Glu692Gly
ENST00000466617.5:c.752A>G ENSP00000420082.1:p.Glu251Gly
ENST00000491190.5:c.974A>G ENSP00000418537.1:p.Glu325Gly
NM_001199642.1:c.1025A>G NP_001186571.1:p.Glu342Gly
NM_183357.2:c.2075A>G NP_899200.1:p.Glu692Gly
XM_005247077.2:c.2075A>G XP_005247134.1:p.Glu692Gly
XM_005247078.1:c.1025A>G XP_005247135.1:p.Glu342Gly
XM_006713483.1:c.974A>G XP_006713546.1:p.Glu325Gly
XM_006713484.1:c.752A>G XP_006713547.1:p.Glu251Gly
XM_011512358.1:c.2075A>G XP_011510660.1:p.Glu692Gly
XM_011512359.1:c.1076A>G XP_011510661.1:p.Glu359Gly
XM_011512360.1:c.986A>G XP_011510662.1:p.Glu329Gly
XM_011512361.1:c.752A>G XP_011510663.1:p.Glu251Gly
XM_005247077.4:c.2075A>G XP_005247134.1:p.Glu692Gly
XM_011512359.2:c.1076A>G XP_011510661.1:p.Glu359Gly
XM_011512360.3:c.986A>G XP_011510662.1:p.Glu329Gly
XM_017005638.1:c.977A>G XP_016861127.1:p.Glu326Gly
XM_017005639.1:c.977A>G XP_016861128.1:p.Glu326Gly
NM_001378259.1:c.2075A>G NP_001365188.1:p.Glu692Gly
NM_183357.3:c.2075A>G MANE Select NP_899200.1:p.Glu692Gly