Canonical Allele Identifier: CA2202928867
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3728832C= , CM000678.2:g.3728832C= GRCh38
NC_000016.9:g.3778833C= , CM000678.1:g.3778833C= GRCh37
NC_000016.8:g.3718834C= NCBI36
NG_009873.1:g.156289G=
NG_009873.2:g.156882G=

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.6215G= MANE Select ENSP00000262367.5:p.Arg2072=
ENST00000262367.9:c.6215G= ENSP00000262367.5:p.Arg2072=
ENST00000382070.7:c.6101G= ENSP00000371502.3:p.Arg2034=
NM_001079846.1:c.6101G= NP_001073315.1:p.Arg2034=
NM_004380.2:c.6215G= NP_004371.2:p.Arg2072=
XM_005255124.3:c.6170G= XP_005255181.1:p.Arg2057=
XM_005255125.3:c.5798G= XP_005255182.1:p.Arg1933=
XM_006720848.2:c.5954G= XP_006720911.1:p.Arg1985=
XM_011522380.1:c.6161G= XP_011520682.1:p.Arg2054=
XM_011522381.1:c.5462G= XP_011520683.1:p.Arg1821=
XM_005255124.4:c.6170G= XP_005255181.1:p.Arg2057=
XM_005255125.4:c.5798G= XP_005255182.1:p.Arg1933=
XM_006720848.3:c.5954G= XP_006720911.1:p.Arg1985=
XM_011522381.2:c.5462G= XP_011520683.1:p.Arg1821=
XM_017022944.1:c.6209G= XP_016878433.1:p.Arg2070=
NM_004380.3:c.6215G= MANE Select NP_004371.2:p.Arg2072=