Canonical Allele Identifier: CA2202944163
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3758810G= , CM000678.2:g.3758810G= GRCh38
NC_000016.9:g.3808811G= , CM000678.1:g.3808811G= GRCh37
NC_000016.8:g.3748812G= NCBI36
NG_009873.1:g.126311C=
NG_009873.2:g.126904C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.3369+44C= MANE Select ENSP00000262367.5:n.3369+44C=
ENST00000262367.9:c.3369+44C= ENSP00000262367.5:n.3369+44C=
ENST00000382070.7:c.3255+44C= ENSP00000371502.3:n.3255+44C=
ENST00000570939.2:c.1974+44C= ENSP00000461002.2:n.1974+44C=
NM_001079846.1:c.3255+44C= NP_001073315.1:n.3255+44C=
NM_004380.2:c.3369+44C= NP_004371.2:n.3369+44C=
XM_005255124.3:c.3324+44C= XP_005255181.1:n.3324+44C=
XM_005255125.3:c.2952+44C= XP_005255182.1:n.2952+44C=
XM_006720848.2:c.3369+44C= XP_006720911.1:n.3369+44C=
XM_011522380.1:c.3315+44C= XP_011520682.1:n.3315+44C=
XM_011522381.1:c.2616+44C= XP_011520683.1:n.2616+44C=
XM_011522382.1:c.3369+44C= XP_011520684.1:n.3369+44C=
XM_005255124.4:c.3324+44C= XP_005255181.1:n.3324+44C=
XM_005255125.4:c.2952+44C= XP_005255182.1:n.2952+44C=
XM_006720848.3:c.3369+44C= XP_006720911.1:n.3369+44C=
XM_011522381.2:c.2616+44C= XP_011520683.1:n.2616+44C=
XM_011522382.3:c.3369+44C= XP_011520684.1:n.3369+44C=
XM_017022944.1:c.3363+44C= XP_016878433.1:n.3363+44C=
NM_004380.3:c.3369+44C= MANE Select NP_004371.2:n.3369+44C=