Canonical Allele Identifier: CA394559239
Gene: CREBBP HGNC NCBI

Linked Data

COSMIC: COSM122356

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3850335C>G , CM000678.2:g.3850335C>G GRCh38
NC_000016.9:g.3900336C>G , CM000678.1:g.3900336C>G GRCh37
NC_000016.8:g.3840337C>G NCBI36
NG_009873.1:g.34786G>C
NG_009873.2:g.35379G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.760G>C MANE Select ENSP00000262367.5:p.Ala254Pro
ENST00000262367.9:c.760G>C ENSP00000262367.5:p.Ala254Pro
ENST00000382070.7:c.760G>C ENSP00000371502.3:p.Ala254Pro
NM_001079846.1:c.760G>C NP_001073315.1:p.Ala254Pro
NM_004380.2:c.760G>C NP_004371.2:p.Ala254Pro
XM_005255124.3:c.760G>C XP_005255181.1:p.Ala254Pro
XM_005255125.3:c.760G>C XP_005255182.1:p.Ala254Pro
XM_006720848.2:c.760G>C XP_006720911.1:p.Ala254Pro
XM_011522380.1:c.706G>C XP_011520682.1:p.Ala236Pro
XM_011522382.1:c.760G>C XP_011520684.1:p.Ala254Pro
XM_005255124.4:c.760G>C XP_005255181.1:p.Ala254Pro
XM_005255125.4:c.760G>C XP_005255182.1:p.Ala254Pro
XM_006720848.3:c.760G>C XP_006720911.1:p.Ala254Pro
XM_011522382.3:c.760G>C XP_011520684.1:p.Ala254Pro
XM_017022944.1:c.760G>C XP_016878433.1:p.Ala254Pro
NM_004380.3:c.760G>C MANE Select NP_004371.2:p.Ala254Pro