Canonical Allele Identifier: CA2202943151
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3757813C= , CM000678.2:g.3757813C= GRCh38
NC_000016.9:g.3807814C= , CM000678.1:g.3807814C= GRCh37
NC_000016.8:g.3747815C= NCBI36
NG_009873.1:g.127308G=
NG_009873.2:g.127901G=

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.3605G= MANE Select ENSP00000262367.5:p.Arg1202=
ENST00000262367.9:c.3605G= ENSP00000262367.5:p.Arg1202=
ENST00000382070.7:c.3491G= ENSP00000371502.3:p.Arg1164=
ENST00000570939.2:c.2210G= ENSP00000461002.2:p.Arg737=
NM_001079846.1:c.3491G= NP_001073315.1:p.Arg1164=
NM_004380.2:c.3605G= NP_004371.2:p.Arg1202=
XM_005255124.3:c.3560G= XP_005255181.1:p.Arg1187=
XM_005255125.3:c.3188G= XP_005255182.1:p.Arg1063=
XM_006720848.2:c.3605G= XP_006720911.1:p.Arg1202=
XM_011522380.1:c.3551G= XP_011520682.1:p.Arg1184=
XM_011522381.1:c.2852G= XP_011520683.1:p.Arg951=
XM_011522382.1:c.3605G= XP_011520684.1:p.Arg1202=
XM_005255124.4:c.3560G= XP_005255181.1:p.Arg1187=
XM_005255125.4:c.3188G= XP_005255182.1:p.Arg1063=
XM_006720848.3:c.3605G= XP_006720911.1:p.Arg1202=
XM_011522381.2:c.2852G= XP_011520683.1:p.Arg951=
XM_011522382.3:c.3605G= XP_011520684.1:p.Arg1202=
XM_017022944.1:c.3599G= XP_016878433.1:p.Arg1200=
NM_004380.3:c.3605G= MANE Select NP_004371.2:p.Arg1202=