Canonical Allele Identifier: CA2202930292
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3745362G= , CM000678.2:g.3745362G= GRCh38
NC_000016.9:g.3795363G= , CM000678.1:g.3795363G= GRCh37
NC_000016.8:g.3735364G= NCBI36
NG_009873.1:g.139759C=
NG_009873.2:g.140352C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.3837-8C= MANE Select ENSP00000262367.5:n.3837-8C=
ENST00000262367.9:c.3837-8C= ENSP00000262367.5:n.3837-8C=
ENST00000382070.7:c.3723-8C= ENSP00000371502.3:n.3723-8C=
ENST00000570939.2:c.2472-8C= ENSP00000461002.2:n.2472-8C=
ENST00000572569.1:n.293C=
ENST00000573517.6:c.143-8C=
NM_001079846.1:c.3723-8C= NP_001073315.1:n.3723-8C=
NM_004380.2:c.3837-8C= NP_004371.2:n.3837-8C=
XM_005255124.3:c.3792-8C= XP_005255181.1:n.3792-8C=
XM_005255125.3:c.3420-8C= XP_005255182.1:n.3420-8C=
XM_006720848.2:c.3837-8C= XP_006720911.1:n.3837-8C=
XM_011522380.1:c.3783-8C= XP_011520682.1:n.3783-8C=
XM_011522381.1:c.3084-8C= XP_011520683.1:n.3084-8C=
XM_005255124.4:c.3792-8C= XP_005255181.1:n.3792-8C=
XM_005255125.4:c.3420-8C= XP_005255182.1:n.3420-8C=
XM_006720848.3:c.3837-8C= XP_006720911.1:n.3837-8C=
XM_011522381.2:c.3084-8C= XP_011520683.1:n.3084-8C=
XM_017022944.1:c.3831-8C= XP_016878433.1:n.3831-8C=
NM_004380.3:c.3837-8C= MANE Select NP_004371.2:n.3837-8C=