Canonical Allele Identifier: CA2202942510
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3757288C= , CM000678.2:g.3757288C= GRCh38
NC_000016.9:g.3807289C= , CM000678.1:g.3807289C= GRCh37
NC_000016.8:g.3747290C= NCBI36
NG_009873.1:g.127833G=
NG_009873.2:g.128426G=

Transcript Alleles

HGVS Amino-acid Change
NM_004380.3:c.3698G= MANE Select NP_004371.2:p.Arg1233=
ENST00000262367.10:c.3698G= MANE Select ENSP00000262367.5:p.Arg1233=
NM_001079846.1:c.3584G= NP_001073315.1:p.Arg1195=
NM_004380.2:c.3698G= NP_004371.2:p.Arg1233=
ENST00000262367.9:c.3698G= ENSP00000262367.5:p.Arg1233=
ENST00000382070.7:c.3584G= ENSP00000371502.3:p.Arg1195=
ENST00000570939.2:c.2303G= ENSP00000461002.2:p.Ser768=
ENST00000573517.6:c.4G=
XM_005255124.3:c.3653G= XP_005255181.1:p.Arg1218=
XM_005255124.4:c.3653G= XP_005255181.1:p.Arg1218=
XM_005255125.3:c.3281G= XP_005255182.1:p.Arg1094=
XM_005255125.4:c.3281G= XP_005255182.1:p.Arg1094=
XM_006720848.2:c.3698G= XP_006720911.1:p.Arg1233=
XM_006720848.3:c.3698G= XP_006720911.1:p.Arg1233=
XM_011522380.1:c.3644G= XP_011520682.1:p.Arg1215=
XM_011522381.1:c.2945G= XP_011520683.1:p.Arg982=
XM_011522381.2:c.2945G= XP_011520683.1:p.Arg982=
XM_011522382.1:c.3698G= XP_011520684.1:p.Arg1233=
XM_011522382.3:c.3698G= XP_011520684.1:p.Arg1233=
XM_017022944.1:c.3692G= XP_016878433.1:p.Arg1231=