Canonical Allele Identifier: CA2840053996
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3739500del , CM000678.2:g.3739500del GRCh38
NC_000016.9:g.3789501del , CM000678.1:g.3789501del GRCh37
NC_000016.8:g.3729502del NCBI36
NG_009873.1:g.145621del
NG_009873.2:g.146214del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.4280+78del MANE Select ENSP00000262367.5:n.4280+78del
ENST00000262367.9:c.4280+78del ENSP00000262367.5:n.4280+78del
ENST00000382070.7:c.4166+78del ENSP00000371502.3:n.4166+78del
ENST00000570939.2:c.2915+78del ENSP00000461002.2:n.2915+78del
ENST00000573517.6:c.664del
ENST00000574740.1:n.215+899del
ENST00000576720.1:n.3217+78del
NM_001079846.1:c.4166+78del NP_001073315.1:n.4166+78del
NM_004380.2:c.4280+78del NP_004371.2:n.4280+78del
XM_005255124.3:c.4235+78del XP_005255181.1:n.4235+78del
XM_005255125.3:c.3863+78del XP_005255182.1:n.3863+78del
XM_006720848.2:c.4133+899del XP_006720911.1:n.4133+899del
XM_011522380.1:c.4226+78del XP_011520682.1:n.4226+78del
XM_011522381.1:c.3527+78del XP_011520683.1:n.3527+78del
XM_005255124.4:c.4235+78del XP_005255181.1:n.4235+78del
XM_005255125.4:c.3863+78del XP_005255182.1:n.3863+78del
XM_006720848.3:c.4133+899del XP_006720911.1:n.4133+899del
XM_011522381.2:c.3527+78del XP_011520683.1:n.3527+78del
XM_017022944.1:c.4274+78del XP_016878433.1:n.4274+78del
NM_004380.3:c.4280+78del MANE Select NP_004371.2:n.4280+78del