Canonical Allele Identifier: CA354221850
Gene: ADCY5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123284642G>A , CM000665.2:g.123284642G>A GRCh38
NC_000003.11:g.123003489G>A , CM000665.1:g.123003489G>A GRCh37
NC_000003.10:g.124486179G>A NCBI36
NG_033882.1:g.168904C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000466617.6:c.2429C>T ENSP00000420082.2:p.Thr810Ile
ENST00000470367.2:c.2717C>T ENSP00000514541.1:p.Thr906Ile
ENST00000483566.2:c.2429C>T ENSP00000420252.2:p.Thr810Ile
ENST00000699714.1:c.2429C>T ENSP00000514539.1:p.Thr810Ile
ENST00000699715.1:c.2429C>T ENSP00000514540.1:p.Thr810Ile
ENST00000699716.1:c.2429C>T ENSP00000514542.1:p.Thr810Ile
ENST00000699717.1:n.2155C>T
ENST00000699718.1:c.3827C>T ENSP00000514543.1:p.Thr1276Ile
ENST00000462833.6:c.3752C>T MANE Select ENSP00000419361.1:p.Thr1251Ile
ENST00000309879.9:c.2702C>T ENSP00000308685.5:p.Thr901Ile
ENST00000462833.5:c.3752C>T ENSP00000419361.1:p.Thr1251Ile
ENST00000478092.1:n.522C>T
ENST00000491190.5:c.2726C>T ENSP00000418537.1:p.Thr909Ile
NM_001199642.1:c.2702C>T NP_001186571.1:p.Thr901Ile
NM_183357.2:c.3752C>T NP_899200.1:p.Thr1251Ile
XM_005247077.2:c.3827C>T XP_005247134.1:p.Thr1276Ile
XM_005247078.1:c.2777C>T XP_005247135.1:p.Thr926Ile
XM_006713483.1:c.2726C>T XP_006713546.1:p.Thr909Ile
XM_006713484.1:c.2504C>T XP_006713547.1:p.Thr835Ile
XM_011512359.1:c.2828C>T XP_011510661.1:p.Thr943Ile
XM_011512360.1:c.2738C>T XP_011510662.1:p.Thr913Ile
XM_011512361.1:c.2504C>T XP_011510663.1:p.Thr835Ile
XM_005247077.4:c.3827C>T XP_005247134.1:p.Thr1276Ile
XM_011512359.2:c.2828C>T XP_011510661.1:p.Thr943Ile
XM_011512360.3:c.2738C>T XP_011510662.1:p.Thr913Ile
XM_017005638.1:c.2729C>T XP_016861127.1:p.Thr910Ile
XM_017005639.1:c.2729C>T XP_016861128.1:p.Thr910Ile
NM_001378259.1:c.3827C>T NP_001365188.1:p.Thr1276Ile
NM_183357.3:c.3752C>T MANE Select NP_899200.1:p.Thr1251Ile