Canonical Allele Identifier: CA2202943156
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3757814G= , CM000678.2:g.3757814G= GRCh38
NC_000016.9:g.3807815G= , CM000678.1:g.3807815G= GRCh37
NC_000016.8:g.3747816G= NCBI36
NG_009873.1:g.127307C=
NG_009873.2:g.127900C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.3604C= MANE Select ENSP00000262367.5:p.Arg1202=
ENST00000262367.9:c.3604C= ENSP00000262367.5:p.Arg1202=
ENST00000382070.7:c.3490C= ENSP00000371502.3:p.Arg1164=
ENST00000570939.2:c.2209C= ENSP00000461002.2:p.Arg737=
NM_001079846.1:c.3490C= NP_001073315.1:p.Arg1164=
NM_004380.2:c.3604C= NP_004371.2:p.Arg1202=
XM_005255124.3:c.3559C= XP_005255181.1:p.Arg1187=
XM_005255125.3:c.3187C= XP_005255182.1:p.Arg1063=
XM_006720848.2:c.3604C= XP_006720911.1:p.Arg1202=
XM_011522380.1:c.3550C= XP_011520682.1:p.Arg1184=
XM_011522381.1:c.2851C= XP_011520683.1:p.Arg951=
XM_011522382.1:c.3604C= XP_011520684.1:p.Arg1202=
XM_005255124.4:c.3559C= XP_005255181.1:p.Arg1187=
XM_005255125.4:c.3187C= XP_005255182.1:p.Arg1063=
XM_006720848.3:c.3604C= XP_006720911.1:p.Arg1202=
XM_011522381.2:c.2851C= XP_011520683.1:p.Arg951=
XM_011522382.3:c.3604C= XP_011520684.1:p.Arg1202=
XM_017022944.1:c.3598C= XP_016878433.1:p.Arg1200=
NM_004380.3:c.3604C= MANE Select NP_004371.2:p.Arg1202=