Canonical Allele Identifier: CA2202971842
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3810671T= , CM000678.2:g.3810671T= GRCh38
NC_000016.9:g.3860672T= , CM000678.1:g.3860672T= GRCh37
NC_000016.8:g.3800673T= NCBI36
NG_009873.1:g.74450A=
NG_009873.2:g.75043A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.907A= MANE Select ENSP00000262367.5:p.Met303=
ENST00000262367.9:c.907A= ENSP00000262367.5:p.Met303=
ENST00000382070.7:c.907A= ENSP00000371502.3:p.Met303=
NM_001079846.1:c.907A= NP_001073315.1:p.Met303=
NM_004380.2:c.907A= NP_004371.2:p.Met303=
XM_005255124.3:c.907A= XP_005255181.1:p.Met303=
XM_005255125.3:c.907A= XP_005255182.1:p.Met303=
XM_006720848.2:c.907A= XP_006720911.1:p.Met303=
XM_011522380.1:c.853A= XP_011520682.1:p.Met285=
XM_011522381.1:c.154A= XP_011520683.1:p.Met52=
XM_011522382.1:c.907A= XP_011520684.1:p.Met303=
XM_005255124.4:c.907A= XP_005255181.1:p.Met303=
XM_005255125.4:c.907A= XP_005255182.1:p.Met303=
XM_006720848.3:c.907A= XP_006720911.1:p.Met303=
XM_011522381.2:c.154A= XP_011520683.1:p.Met52=
XM_011522382.3:c.907A= XP_011520684.1:p.Met303=
XM_017022944.1:c.907A= XP_016878433.1:p.Met303=
NM_004380.3:c.907A= MANE Select NP_004371.2:p.Met303=