Canonical Allele Identifier: CA2631424057
Gene: CREBBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3757795del , CM000678.2:g.3757795del GRCh38
NC_000016.9:g.3807796del , CM000678.1:g.3807796del GRCh37
NC_000016.8:g.3747797del NCBI36
NG_009873.1:g.127330del
NG_009873.2:g.127923del

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.3609+18del MANE Select ENSP00000262367.5:n.3609+18del
ENST00000262367.9:c.3609+18del ENSP00000262367.5:n.3609+18del
ENST00000382070.7:c.3495+18del ENSP00000371502.3:n.3495+18del
ENST00000570939.2:c.2214+18del ENSP00000461002.2:n.2214+18del
NM_001079846.1:c.3495+18del NP_001073315.1:n.3495+18del
NM_004380.2:c.3609+18del NP_004371.2:n.3609+18del
XM_005255124.3:c.3564+18del XP_005255181.1:n.3564+18del
XM_005255125.3:c.3192+18del XP_005255182.1:n.3192+18del
XM_006720848.2:c.3609+18del XP_006720911.1:n.3609+18del
XM_011522380.1:c.3555+18del XP_011520682.1:n.3555+18del
XM_011522381.1:c.2856+18del XP_011520683.1:n.2856+18del
XM_011522382.1:c.3609+18del XP_011520684.1:n.3609+18del
XM_005255124.4:c.3564+18del XP_005255181.1:n.3564+18del
XM_005255125.4:c.3192+18del XP_005255182.1:n.3192+18del
XM_006720848.3:c.3609+18del XP_006720911.1:n.3609+18del
XM_011522381.2:c.2856+18del XP_011520683.1:n.2856+18del
XM_011522382.3:c.3609+18del XP_011520684.1:n.3609+18del
XM_017022944.1:c.3603+18del XP_016878433.1:n.3603+18del
NM_004380.3:c.3609+18del MANE Select NP_004371.2:n.3609+18del