Canonical Allele Identifier: CA2202928367
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3727849A= , CM000678.2:g.3727849A= GRCh38
NC_000016.9:g.3777850A= , CM000678.1:g.3777850A= GRCh37
NC_000016.8:g.3717851A= NCBI36
NG_009873.1:g.157272T=
NG_009873.2:g.157865T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.7198T= MANE Select ENSP00000262367.5:p.Leu2400=
ENST00000262367.9:c.7198T= ENSP00000262367.5:p.Leu2400=
ENST00000382070.7:c.7084T= ENSP00000371502.3:p.Leu2362=
NM_001079846.1:c.7084T= NP_001073315.1:p.Leu2362=
NM_004380.2:c.7198T= NP_004371.2:p.Leu2400=
XM_005255124.3:c.7153T= XP_005255181.1:p.Leu2385=
XM_005255125.3:c.6781T= XP_005255182.1:p.Leu2261=
XM_006720848.2:c.6937T= XP_006720911.1:p.Leu2313=
XM_011522380.1:c.7144T= XP_011520682.1:p.Leu2382=
XM_011522381.1:c.6445T= XP_011520683.1:p.Leu2149=
XM_005255124.4:c.7153T= XP_005255181.1:p.Leu2385=
XM_005255125.4:c.6781T= XP_005255182.1:p.Leu2261=
XM_006720848.3:c.6937T= XP_006720911.1:p.Leu2313=
XM_011522381.2:c.6445T= XP_011520683.1:p.Leu2149=
XM_017022944.1:c.7192T= XP_016878433.1:p.Leu2398=
NM_004380.3:c.7198T= MANE Select NP_004371.2:p.Leu2400=