Canonical Allele Identifier: CA354222490
Gene: ADCY5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123352436T>C , CM000665.2:g.123352436T>C GRCh38
NC_000003.11:g.123071283T>C , CM000665.1:g.123071283T>C GRCh37
NC_000003.10:g.124553973T>C NCBI36
NG_033882.1:g.101110A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000466617.6:c.-44A>G ENSP00000420082.2:n.-44A>G
ENST00000470367.2:c.245A>G ENSP00000514541.1:p.Gln82Arg
ENST00000483566.2:c.-44A>G ENSP00000420252.2:n.-44A>G
ENST00000699714.1:c.-44A>G ENSP00000514539.1:n.-44A>G
ENST00000699715.1:c.-44A>G ENSP00000514540.1:n.-44A>G
ENST00000699716.1:c.-44A>G ENSP00000514542.1:n.-44A>G
ENST00000699718.1:c.1280A>G ENSP00000514543.1:p.Gln427Arg
ENST00000462833.6:c.1280A>G MANE Select ENSP00000419361.1:p.Gln427Arg
ENST00000309879.9:c.230A>G ENSP00000308685.5:p.Gln77Arg
ENST00000462833.5:c.1280A>G ENSP00000419361.1:p.Gln427Arg
ENST00000466617.5:c.-44A>G ENSP00000420082.1:n.-44A>G
ENST00000476455.1:c.184A>G ENSP00000417789.1:p.Ser62Gly
ENST00000483566.1:c.-44A>G ENSP00000420252.1:n.-44A>G
ENST00000491190.5:c.179A>G ENSP00000418537.1:p.Gln60Arg
NM_001199642.1:c.230A>G NP_001186571.1:p.Gln77Arg
NM_183357.2:c.1280A>G NP_899200.1:p.Gln427Arg
XM_005247077.2:c.1280A>G XP_005247134.1:p.Gln427Arg
XM_005247078.1:c.230A>G XP_005247135.1:p.Gln77Arg
XM_006713483.1:c.179A>G XP_006713546.1:p.Gln60Arg
XM_006713484.1:c.-44A>G XP_006713547.1:n.-44A>G
XM_011512358.1:c.1280A>G XP_011510660.1:p.Gln427Arg
XM_011512359.1:c.281A>G XP_011510661.1:p.Gln94Arg
XM_011512360.1:c.191A>G XP_011510662.1:p.Gln64Arg
XM_011512361.1:c.-44A>G XP_011510663.1:n.-44A>G
XM_005247077.4:c.1280A>G XP_005247134.1:p.Gln427Arg
XM_011512359.2:c.281A>G XP_011510661.1:p.Gln94Arg
XM_011512360.3:c.191A>G XP_011510662.1:p.Gln64Arg
XM_017005638.1:c.182A>G XP_016861127.1:p.Gln61Arg
XM_017005639.1:c.182A>G XP_016861128.1:p.Gln61Arg
NM_001378259.1:c.1280A>G NP_001365188.1:p.Gln427Arg
NM_183357.3:c.1280A>G MANE Select NP_899200.1:p.Gln427Arg