Canonical Allele Identifier: CA394560527
Gene: CREBBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3792001C>G , CM000678.2:g.3792001C>G GRCh38
NC_000016.9:g.3842002C>G , CM000678.1:g.3842002C>G GRCh37
NC_000016.8:g.3782003C>G NCBI36
NG_009873.1:g.93120G>C
NG_009873.2:g.93713G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.1310G>C MANE Select ENSP00000262367.5:p.Ser437Thr
ENST00000262367.9:c.1310G>C ENSP00000262367.5:p.Ser437Thr
ENST00000382070.7:c.1216+1385G>C ENSP00000371502.3:n.1216+1385G>C
NM_001079846.1:c.1216+1385G>C NP_001073315.1:n.1216+1385G>C
NM_004380.2:c.1310G>C NP_004371.2:p.Ser437Thr
XM_005255124.3:c.1310G>C XP_005255181.1:p.Ser437Thr
XM_005255125.3:c.1310G>C XP_005255182.1:p.Ser437Thr
XM_006720848.2:c.1310G>C XP_006720911.1:p.Ser437Thr
XM_011522380.1:c.1256G>C XP_011520682.1:p.Ser419Thr
XM_011522381.1:c.557G>C XP_011520683.1:p.Ser186Thr
XM_011522382.1:c.1310G>C XP_011520684.1:p.Ser437Thr
XM_005255124.4:c.1310G>C XP_005255181.1:p.Ser437Thr
XM_005255125.4:c.1310G>C XP_005255182.1:p.Ser437Thr
XM_006720848.3:c.1310G>C XP_006720911.1:p.Ser437Thr
XM_011522381.2:c.557G>C XP_011520683.1:p.Ser186Thr
XM_011522382.3:c.1310G>C XP_011520684.1:p.Ser437Thr
XM_017022944.1:c.1310G>C XP_016878433.1:p.Ser437Thr
NM_004380.3:c.1310G>C MANE Select NP_004371.2:p.Ser437Thr