Canonical Allele Identifier: CA2202940835
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3740453C= , CM000678.2:g.3740453C= GRCh38
NC_000016.9:g.3790454C= , CM000678.1:g.3790454C= GRCh37
NC_000016.8:g.3730455C= NCBI36
NG_009873.1:g.144668G=
NG_009873.2:g.145261G=

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.4079G= MANE Select ENSP00000262367.5:p.Arg1360=
ENST00000262367.9:c.4079G= ENSP00000262367.5:p.Arg1360=
ENST00000382070.7:c.3965G= ENSP00000371502.3:p.Arg1322=
ENST00000570939.2:c.2714G= ENSP00000461002.2:p.Arg905=
ENST00000572569.1:n.543G=
ENST00000573517.6:c.385G=
ENST00000574740.1:n.161G=
ENST00000576720.1:n.3016G=
NM_001079846.1:c.3965G= NP_001073315.1:p.Arg1322=
NM_004380.2:c.4079G= NP_004371.2:p.Arg1360=
XM_005255124.3:c.4034G= XP_005255181.1:p.Arg1345=
XM_005255125.3:c.3662G= XP_005255182.1:p.Arg1221=
XM_006720848.2:c.4079G= XP_006720911.1:p.Arg1360=
XM_011522380.1:c.4025G= XP_011520682.1:p.Arg1342=
XM_011522381.1:c.3326G= XP_011520683.1:p.Arg1109=
XM_005255124.4:c.4034G= XP_005255181.1:p.Arg1345=
XM_005255125.4:c.3662G= XP_005255182.1:p.Arg1221=
XM_006720848.3:c.4079G= XP_006720911.1:p.Arg1360=
XM_011522381.2:c.3326G= XP_011520683.1:p.Arg1109=
XM_017022944.1:c.4073G= XP_016878433.1:p.Arg1358=
NM_004380.3:c.4079G= MANE Select NP_004371.2:p.Arg1360=