Canonical Allele Identifier: CA1052997448
Gene: ADCY5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123377948_123377949insAAACAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000665.2:g.123377948_123377949insAAACAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA GRCh38
NC_000003.11:g.123096795_123096796insAAACAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000665.1:g.123096795_123096796insAAACAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA GRCh37
NC_000003.10:g.124579485_124579486insAAACAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA NCBI36
NG_033882.1:g.75616_75617insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000466617.6:c.-189-25349_-189-25348insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT ENSP00000420082.2:n.-189-25349_-189-25348insTTTTTTTTTTTTTTTTT...
ENST00000470367.2:c.100-25349_100-25348insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT ENSP00000514541.1:n.100-25349_100-25348insTTTTTTTTTTTTTTTTTTC...
ENST00000483566.2:c.-189-25349_-189-25348insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT ENSP00000420252.2:n.-189-25349_-189-25348insTTTTTTTTTTTTTTTTT...
ENST00000699714.1:c.-189-25349_-189-25348insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT ENSP00000514539.1:n.-189-25349_-189-25348insTTTTTTTTTTTTTTTTT...
ENST00000699715.1:c.-189-25349_-189-25348insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT ENSP00000514540.1:n.-189-25349_-189-25348insTTTTTTTTTTTTTTTTT...
ENST00000699716.1:c.-189-25349_-189-25348insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT ENSP00000514542.1:n.-189-25349_-189-25348insTTTTTTTTTTTTTTTTT...
ENST00000699718.1:c.1135-25349_1135-25348insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT ENSP00000514543.1:n.1135-25349_1135-25348insTTTTTTTTTTTTTTTTT...
ENST00000462833.6:c.1135-25349_1135-25348insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT MANE Select ENSP00000419361.1:n.1135-25349_1135-25348insTTTTTTTTTTTTTTTTT...
ENST00000309879.9:c.85-25349_85-25348insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT ENSP00000308685.5:n.85-25349_85-25348insTTTTTTTTTTTTTTTTTTCTT...
ENST00000462833.5:c.1135-25349_1135-25348insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT ENSP00000419361.1:n.1135-25349_1135-25348insTTTTTTTTTTTTTTTTT...
ENST00000466617.5:c.-189-25349_-189-25348insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT ENSP00000420082.1:n.-189-25349_-189-25348insTTTTTTTTTTTTTTTTT...
ENST00000470367.1:n.430-25349_430-25348insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT
ENST00000476455.1:c.-109-9884_-109-9883insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT ENSP00000417789.1:n.-109-9884_-109-9883insTTTTTTTTTTTTTTTTTTC...
ENST00000483566.1:c.-189-25349_-189-25348insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT ENSP00000420252.1:n.-189-25349_-189-25348insTTTTTTTTTTTTTTTTT...
ENST00000491190.5:c.-109-9884_-109-9883insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT ENSP00000418537.1:n.-109-9884_-109-9883insTTTTTTTTTTTTTTTTTTC...
NM_001199642.1:c.85-25349_85-25348insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT NP_001186571.1:n.85-25349_85-25348insTTTTTTTTTTTTTTTTTTCTTTTT...
NM_183357.2:c.1135-25349_1135-25348insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT NP_899200.1:n.1135-25349_1135-25348insTTTTTTTTTTTTTTTTTTCTTTT...
XM_005247077.2:c.1135-25349_1135-25348insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT XP_005247134.1:n.1135-25349_1135-25348insTTTTTTTTTTTTTTTTTTCT...
XM_005247078.1:c.85-25349_85-25348insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT XP_005247135.1:n.85-25349_85-25348insTTTTTTTTTTTTTTTTTTCTTTTT...
XM_006713484.1:c.-189-25349_-189-25348insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT XP_006713547.1:n.-189-25349_-189-25348insTTTTTTTTTTTTTTTTTTCT...
XM_011512358.1:c.1135-25349_1135-25348insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT XP_011510660.1:n.1135-25349_1135-25348insTTTTTTTTTTTTTTTTTTCT...
XM_011512359.1:c.136-25349_136-25348insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT XP_011510661.1:n.136-25349_136-25348insTTTTTTTTTTTTTTTTTTCTTT...
XM_011512361.1:c.-189-25349_-189-25348insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT XP_011510663.1:n.-189-25349_-189-25348insTTTTTTTTTTTTTTTTTTCT...
XM_005247077.4:c.1135-25349_1135-25348insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT XP_005247134.1:n.1135-25349_1135-25348insTTTTTTTTTTTTTTTTTTCT...
XM_011512359.2:c.136-25349_136-25348insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT XP_011510661.1:n.136-25349_136-25348insTTTTTTTTTTTTTTTTTTCTTT...
XM_017005638.1:c.36+12411_36+12412insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT XP_016861127.1:n.36+12411_36+12412insTTTTTTTTTTTTTTTTTTCTTTTT...
XM_017005639.1:c.36+12865_36+12866insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT XP_016861128.1:n.36+12865_36+12866insTTTTTTTTTTTTTTTTTTCTTTTT...
NM_001378259.1:c.1135-25349_1135-25348insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT NP_001365188.1:n.1135-25349_1135-25348insTTTTTTTTTTTTTTTTTTCT...
NM_183357.3:c.1135-25349_1135-25348insTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT MANE Select NP_899200.1:n.1135-25349_1135-25348insTTTTTTTTTTTTTTTTTTCTTTT...