Canonical Allele Identifier: CA2202939681
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3739504G= , CM000678.2:g.3739504G= GRCh38
NC_000016.9:g.3789505G= , CM000678.1:g.3789505G= GRCh37
NC_000016.8:g.3729506G= NCBI36
NG_009873.1:g.145617C=
NG_009873.2:g.146210C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.4280+74C= MANE Select ENSP00000262367.5:n.4280+74C=
ENST00000262367.9:c.4280+74C= ENSP00000262367.5:n.4280+74C=
ENST00000382070.7:c.4166+74C= ENSP00000371502.3:n.4166+74C=
ENST00000570939.2:c.2915+74C= ENSP00000461002.2:n.2915+74C=
ENST00000573517.6:c.660C=
ENST00000574740.1:n.215+895C=
ENST00000576720.1:n.3217+74C=
NM_001079846.1:c.4166+74C= NP_001073315.1:n.4166+74C=
NM_004380.2:c.4280+74C= NP_004371.2:n.4280+74C=
XM_005255124.3:c.4235+74C= XP_005255181.1:n.4235+74C=
XM_005255125.3:c.3863+74C= XP_005255182.1:n.3863+74C=
XM_006720848.2:c.4133+895C= XP_006720911.1:n.4133+895C=
XM_011522380.1:c.4226+74C= XP_011520682.1:n.4226+74C=
XM_011522381.1:c.3527+74C= XP_011520683.1:n.3527+74C=
XM_005255124.4:c.4235+74C= XP_005255181.1:n.4235+74C=
XM_005255125.4:c.3863+74C= XP_005255182.1:n.3863+74C=
XM_006720848.3:c.4133+895C= XP_006720911.1:n.4133+895C=
XM_011522381.2:c.3527+74C= XP_011520683.1:n.3527+74C=
XM_017022944.1:c.4274+74C= XP_016878433.1:n.4274+74C=
NM_004380.3:c.4280+74C= MANE Select NP_004371.2:n.4280+74C=