Canonical Allele Identifier: CA2202936661
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3736739G= , CM000678.2:g.3736739G= GRCh38
NC_000016.9:g.3786740G= , CM000678.1:g.3786740G= GRCh37
NC_000016.8:g.3726741G= NCBI36
NG_009873.1:g.148382C=
NG_009873.2:g.148975C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.4471C= MANE Select ENSP00000262367.5:p.Gln1491=
ENST00000262367.9:c.4471C= ENSP00000262367.5:p.Gln1491=
ENST00000382070.7:c.4357C= ENSP00000371502.3:p.Gln1453=
ENST00000570939.2:c.3106C= ENSP00000461002.2:p.Gln1036=
ENST00000571763.5:n.261C=
ENST00000574740.1:n.292C=
ENST00000576720.1:n.3294C=
NM_001079846.1:c.4357C= NP_001073315.1:p.Gln1453=
NM_004380.2:c.4471C= NP_004371.2:p.Gln1491=
XM_005255124.3:c.4426C= XP_005255181.1:p.Gln1476=
XM_005255125.3:c.4054C= XP_005255182.1:p.Gln1352=
XM_006720848.2:c.4210C= XP_006720911.1:p.Gln1404=
XM_011522380.1:c.4417C= XP_011520682.1:p.Gln1473=
XM_011522381.1:c.3718C= XP_011520683.1:p.Gln1240=
XM_005255124.4:c.4426C= XP_005255181.1:p.Gln1476=
XM_005255125.4:c.4054C= XP_005255182.1:p.Gln1352=
XM_006720848.3:c.4210C= XP_006720911.1:p.Gln1404=
XM_011522381.2:c.3718C= XP_011520683.1:p.Gln1240=
XM_017022944.1:c.4465C= XP_016878433.1:p.Gln1489=
NM_004380.3:c.4471C= MANE Select NP_004371.2:p.Gln1491=