Canonical Allele Identifier: CA2202940629
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs754655634

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3740267dup , CM000678.2:g.3740267dup GRCh38
NC_000016.9:g.3790268dup , CM000678.1:g.3790268dup GRCh37
NC_000016.8:g.3730269dup NCBI36
NG_009873.1:g.144858dup
NG_009873.2:g.145451dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.4133+136dup MANE Select ENSP00000262367.5:n.4133+136dup
ENST00000262367.9:c.4133+136dup ENSP00000262367.5:n.4133+136dup
ENST00000382070.7:c.4019+136dup ENSP00000371502.3:n.4019+136dup
ENST00000570939.2:c.2768+136dup ENSP00000461002.2:n.2768+136dup
ENST00000573517.6:c.439+136dup
ENST00000574740.1:n.215+136dup
ENST00000576720.1:n.3070+136dup
NM_001079846.1:c.4019+136dup NP_001073315.1:n.4019+136dup
NM_004380.2:c.4133+136dup NP_004371.2:n.4133+136dup
XM_005255124.3:c.4088+136dup XP_005255181.1:n.4088+136dup
XM_005255125.3:c.3716+136dup XP_005255182.1:n.3716+136dup
XM_006720848.2:c.4133+136dup XP_006720911.1:n.4133+136dup
XM_011522380.1:c.4079+136dup XP_011520682.1:n.4079+136dup
XM_011522381.1:c.3380+136dup XP_011520683.1:n.3380+136dup
XM_005255124.4:c.4088+136dup XP_005255181.1:n.4088+136dup
XM_005255125.4:c.3716+136dup XP_005255182.1:n.3716+136dup
XM_006720848.3:c.4133+136dup XP_006720911.1:n.4133+136dup
XM_011522381.2:c.3380+136dup XP_011520683.1:n.3380+136dup
XM_017022944.1:c.4127+136dup XP_016878433.1:n.4127+136dup
NM_004380.3:c.4133+136dup MANE Select NP_004371.2:n.4133+136dup