Canonical Allele Identifier: CA2695222693
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3792055del , CM000678.2:g.3792055del GRCh38
NC_000016.9:g.3842056del , CM000678.1:g.3842056del GRCh37
NC_000016.8:g.3782057del NCBI36
NG_009873.1:g.93067del
NG_009873.2:g.93660del

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.1257del MANE Select ENSP00000262367.5:p.Trp419Ter
ENST00000262367.9:c.1257del ENSP00000262367.5:p.Trp419Ter
ENST00000382070.7:c.1216+1332del ENSP00000371502.3:n.1216+1332del
NM_001079846.1:c.1216+1332del NP_001073315.1:n.1216+1332del
NM_004380.2:c.1257del NP_004371.2:p.Trp419Ter
XM_005255124.3:c.1257del XP_005255181.1:p.Trp419Ter
XM_005255125.3:c.1257del XP_005255182.1:p.Trp419Ter
XM_006720848.2:c.1257del XP_006720911.1:p.Trp419Ter
XM_011522380.1:c.1203del XP_011520682.1:p.Trp401Ter
XM_011522381.1:c.504del XP_011520683.1:p.Trp168Ter
XM_011522382.1:c.1257del XP_011520684.1:p.Trp419Ter
XM_005255124.4:c.1257del XP_005255181.1:p.Trp419Ter
XM_005255125.4:c.1257del XP_005255182.1:p.Trp419Ter
XM_006720848.3:c.1257del XP_006720911.1:p.Trp419Ter
XM_011522381.2:c.504del XP_011520683.1:p.Trp168Ter
XM_011522382.3:c.1257del XP_011520684.1:p.Trp419Ter
XM_017022944.1:c.1257del XP_016878433.1:p.Trp419Ter
NM_004380.3:c.1257del MANE Select NP_004371.2:p.Trp419Ter