Canonical Allele Identifier: CA2202930916
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3746091T= , CM000678.2:g.3746091T= GRCh38
NC_000016.9:g.3796092T= , CM000678.1:g.3796092T= GRCh37
NC_000016.8:g.3736093T= NCBI36
NG_009873.1:g.139030A=
NG_009873.2:g.139623A=

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.3837-737A= MANE Select ENSP00000262367.5:n.3837-737A=
ENST00000638158.1:n.58-496A=
ENST00000262367.9:c.3837-737A= ENSP00000262367.5:n.3837-737A=
ENST00000382070.7:c.3723-737A= ENSP00000371502.3:n.3723-737A=
ENST00000570939.2:c.2472-737A= ENSP00000461002.2:n.2472-737A=
ENST00000573517.6:c.143-737A=
NM_001079846.1:c.3723-737A= NP_001073315.1:n.3723-737A=
NM_004380.2:c.3837-737A= NP_004371.2:n.3837-737A=
XM_005255124.3:c.3792-737A= XP_005255181.1:n.3792-737A=
XM_005255125.3:c.3420-737A= XP_005255182.1:n.3420-737A=
XM_006720848.2:c.3837-737A= XP_006720911.1:n.3837-737A=
XM_011522380.1:c.3783-737A= XP_011520682.1:n.3783-737A=
XM_011522381.1:c.3084-737A= XP_011520683.1:n.3084-737A=
XM_011522382.1:c.3837-496A= XP_011520684.1:n.3837-496A=
XM_005255124.4:c.3792-737A= XP_005255181.1:n.3792-737A=
XM_005255125.4:c.3420-737A= XP_005255182.1:n.3420-737A=
XM_006720848.3:c.3837-737A= XP_006720911.1:n.3837-737A=
XM_011522381.2:c.3084-737A= XP_011520683.1:n.3084-737A=
XM_011522382.3:c.3837-496A= XP_011520684.1:n.3837-496A=
XM_017022944.1:c.3831-737A= XP_016878433.1:n.3831-737A=
NM_004380.3:c.3837-737A= MANE Select NP_004371.2:n.3837-737A=