Canonical Allele Identifier: CA394557681
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3782810G>A , CM000678.2:g.3782810G>A GRCh38
NC_000016.9:g.3832811G>A , CM000678.1:g.3832811G>A GRCh37
NC_000016.8:g.3772812G>A NCBI36
NG_009873.1:g.102311C>T
NG_009873.2:g.102904C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.1447C>T MANE Select ENSP00000262367.5:p.Arg483Ter
ENST00000262367.9:c.1447C>T ENSP00000262367.5:p.Arg483Ter
ENST00000382070.7:c.1333C>T ENSP00000371502.3:p.Arg445Ter
ENST00000570939.2:c.52C>T ENSP00000461002.2:p.Arg18Ter
NM_001079846.1:c.1333C>T NP_001073315.1:p.Arg445Ter
NM_004380.2:c.1447C>T NP_004371.2:p.Arg483Ter
XM_005255124.3:c.1447C>T XP_005255181.1:p.Arg483Ter
XM_005255125.3:c.1447C>T XP_005255182.1:p.Arg483Ter
XM_006720848.2:c.1447C>T XP_006720911.1:p.Arg483Ter
XM_011522380.1:c.1393C>T XP_011520682.1:p.Arg465Ter
XM_011522381.1:c.694C>T XP_011520683.1:p.Arg232Ter
XM_011522382.1:c.1447C>T XP_011520684.1:p.Arg483Ter
XM_005255124.4:c.1447C>T XP_005255181.1:p.Arg483Ter
XM_005255125.4:c.1447C>T XP_005255182.1:p.Arg483Ter
XM_006720848.3:c.1447C>T XP_006720911.1:p.Arg483Ter
XM_011522381.2:c.694C>T XP_011520683.1:p.Arg232Ter
XM_011522382.3:c.1447C>T XP_011520684.1:p.Arg483Ter
XM_017022944.1:c.1447C>T XP_016878433.1:p.Arg483Ter
NM_004380.3:c.1447C>T MANE Select NP_004371.2:p.Arg483Ter