Canonical Allele Identifier: CA2202940828
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3740444G= , CM000678.2:g.3740444G= GRCh38
NC_000016.9:g.3790445G= , CM000678.1:g.3790445G= GRCh37
NC_000016.8:g.3730446G= NCBI36
NG_009873.1:g.144677C=
NG_009873.2:g.145270C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.4088C= MANE Select ENSP00000262367.5:p.Ala1363=
ENST00000262367.9:c.4088C= ENSP00000262367.5:p.Ala1363=
ENST00000382070.7:c.3974C= ENSP00000371502.3:p.Ala1325=
ENST00000570939.2:c.2723C= ENSP00000461002.2:p.Ala908=
ENST00000572569.1:n.552C=
ENST00000573517.6:c.394C=
ENST00000574740.1:n.170C=
ENST00000576720.1:n.3025C=
NM_001079846.1:c.3974C= NP_001073315.1:p.Ala1325=
NM_004380.2:c.4088C= NP_004371.2:p.Ala1363=
XM_005255124.3:c.4043C= XP_005255181.1:p.Ala1348=
XM_005255125.3:c.3671C= XP_005255182.1:p.Ala1224=
XM_006720848.2:c.4088C= XP_006720911.1:p.Ala1363=
XM_011522380.1:c.4034C= XP_011520682.1:p.Ala1345=
XM_011522381.1:c.3335C= XP_011520683.1:p.Ala1112=
XM_005255124.4:c.4043C= XP_005255181.1:p.Ala1348=
XM_005255125.4:c.3671C= XP_005255182.1:p.Ala1224=
XM_006720848.3:c.4088C= XP_006720911.1:p.Ala1363=
XM_011522381.2:c.3335C= XP_011520683.1:p.Ala1112=
XM_017022944.1:c.4082C= XP_016878433.1:p.Ala1361=
NM_004380.3:c.4088C= MANE Select NP_004371.2:p.Ala1363=