Canonical Allele Identifier: CA2202930931
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3746114C= , CM000678.2:g.3746114C= GRCh38
NC_000016.9:g.3796115C= , CM000678.1:g.3796115C= GRCh37
NC_000016.8:g.3736116C= NCBI36
NG_009873.1:g.139007G=
NG_009873.2:g.139600G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.3837-760G= MANE Select ENSP00000262367.5:n.3837-760G=
ENST00000638158.1:n.58-519G=
ENST00000262367.9:c.3837-760G= ENSP00000262367.5:n.3837-760G=
ENST00000382070.7:c.3723-760G= ENSP00000371502.3:n.3723-760G=
ENST00000570939.2:c.2472-760G= ENSP00000461002.2:n.2472-760G=
ENST00000573517.6:c.143-760G=
NM_001079846.1:c.3723-760G= NP_001073315.1:n.3723-760G=
NM_004380.2:c.3837-760G= NP_004371.2:n.3837-760G=
XM_005255124.3:c.3792-760G= XP_005255181.1:n.3792-760G=
XM_005255125.3:c.3420-760G= XP_005255182.1:n.3420-760G=
XM_006720848.2:c.3837-760G= XP_006720911.1:n.3837-760G=
XM_011522380.1:c.3783-760G= XP_011520682.1:n.3783-760G=
XM_011522381.1:c.3084-760G= XP_011520683.1:n.3084-760G=
XM_011522382.1:c.3837-519G= XP_011520684.1:n.3837-519G=
XM_005255124.4:c.3792-760G= XP_005255181.1:n.3792-760G=
XM_005255125.4:c.3420-760G= XP_005255182.1:n.3420-760G=
XM_006720848.3:c.3837-760G= XP_006720911.1:n.3837-760G=
XM_011522381.2:c.3084-760G= XP_011520683.1:n.3084-760G=
XM_011522382.3:c.3837-519G= XP_011520684.1:n.3837-519G=
XM_017022944.1:c.3831-760G= XP_016878433.1:n.3831-760G=
NM_004380.3:c.3837-760G= MANE Select NP_004371.2:n.3837-760G=