Canonical Allele Identifier: CA2631401488
Gene: CREBBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3736540del , CM000678.2:g.3736540del GRCh38
NC_000016.9:g.3786541del , CM000678.1:g.3786541del GRCh37
NC_000016.8:g.3726542del NCBI36
NG_009873.1:g.148582del
NG_009873.2:g.149175del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.4560+111del MANE Select ENSP00000262367.5:n.4560+111del
ENST00000262367.9:c.4560+111del ENSP00000262367.5:n.4560+111del
ENST00000382070.7:c.4446+111del ENSP00000371502.3:n.4446+111del
ENST00000570939.2:c.3195+111del ENSP00000461002.2:n.3195+111del
ENST00000571763.5:n.350+111del
ENST00000574740.1:n.492del
ENST00000576720.1:n.3383+111del
NM_001079846.1:c.4446+111del NP_001073315.1:n.4446+111del
NM_004380.2:c.4560+111del NP_004371.2:n.4560+111del
XM_005255124.3:c.4515+111del XP_005255181.1:n.4515+111del
XM_005255125.3:c.4143+111del XP_005255182.1:n.4143+111del
XM_006720848.2:c.4299+111del XP_006720911.1:n.4299+111del
XM_011522380.1:c.4506+111del XP_011520682.1:n.4506+111del
XM_011522381.1:c.3807+111del XP_011520683.1:n.3807+111del
XM_005255124.4:c.4515+111del XP_005255181.1:n.4515+111del
XM_005255125.4:c.4143+111del XP_005255182.1:n.4143+111del
XM_006720848.3:c.4299+111del XP_006720911.1:n.4299+111del
XM_011522381.2:c.3807+111del XP_011520683.1:n.3807+111del
XM_017022944.1:c.4554+111del XP_016878433.1:n.4554+111del
NM_004380.3:c.4560+111del MANE Select NP_004371.2:n.4560+111del