Canonical Allele Identifier: CA2202936425
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3736564C= , CM000678.2:g.3736564C= GRCh38
NC_000016.9:g.3786565C= , CM000678.1:g.3786565C= GRCh37
NC_000016.8:g.3726566C= NCBI36
NG_009873.1:g.148557G=
NG_009873.2:g.149150G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.4560+86G= MANE Select ENSP00000262367.5:n.4560+86G=
ENST00000262367.9:c.4560+86G= ENSP00000262367.5:n.4560+86G=
ENST00000382070.7:c.4446+86G= ENSP00000371502.3:n.4446+86G=
ENST00000570939.2:c.3195+86G= ENSP00000461002.2:n.3195+86G=
ENST00000571763.5:n.350+86G=
ENST00000574740.1:n.467G=
ENST00000576720.1:n.3383+86G=
NM_001079846.1:c.4446+86G= NP_001073315.1:n.4446+86G=
NM_004380.2:c.4560+86G= NP_004371.2:n.4560+86G=
XM_005255124.3:c.4515+86G= XP_005255181.1:n.4515+86G=
XM_005255125.3:c.4143+86G= XP_005255182.1:n.4143+86G=
XM_006720848.2:c.4299+86G= XP_006720911.1:n.4299+86G=
XM_011522380.1:c.4506+86G= XP_011520682.1:n.4506+86G=
XM_011522381.1:c.3807+86G= XP_011520683.1:n.3807+86G=
XM_005255124.4:c.4515+86G= XP_005255181.1:n.4515+86G=
XM_005255125.4:c.4143+86G= XP_005255182.1:n.4143+86G=
XM_006720848.3:c.4299+86G= XP_006720911.1:n.4299+86G=
XM_011522381.2:c.3807+86G= XP_011520683.1:n.3807+86G=
XM_017022944.1:c.4554+86G= XP_016878433.1:n.4554+86G=
NM_004380.3:c.4560+86G= MANE Select NP_004371.2:n.4560+86G=