Canonical Allele Identifier: CA2202937113
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3737150G= , CM000678.2:g.3737150G= GRCh38
NC_000016.9:g.3787151G= , CM000678.1:g.3787151G= GRCh37
NC_000016.8:g.3727152G= NCBI36
NG_009873.1:g.147971C=
NG_009873.2:g.148564C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.4395-335C= MANE Select ENSP00000262367.5:n.4395-335C=
ENST00000262367.9:c.4395-335C= ENSP00000262367.5:n.4395-335C=
ENST00000382070.7:c.4281-335C= ENSP00000371502.3:n.4281-335C=
ENST00000570939.2:c.3030-335C= ENSP00000461002.2:n.3030-335C=
ENST00000574740.1:n.216-335C=
ENST00000576720.1:n.3218-335C=
NM_001079846.1:c.4281-335C= NP_001073315.1:n.4281-335C=
NM_004380.2:c.4395-335C= NP_004371.2:n.4395-335C=
XM_005255124.3:c.4350-335C= XP_005255181.1:n.4350-335C=
XM_005255125.3:c.3978-335C= XP_005255182.1:n.3978-335C=
XM_006720848.2:c.4134-335C= XP_006720911.1:n.4134-335C=
XM_011522380.1:c.4341-335C= XP_011520682.1:n.4341-335C=
XM_011522381.1:c.3642-335C= XP_011520683.1:n.3642-335C=
XM_005255124.4:c.4350-335C= XP_005255181.1:n.4350-335C=
XM_005255125.4:c.3978-335C= XP_005255182.1:n.3978-335C=
XM_006720848.3:c.4134-335C= XP_006720911.1:n.4134-335C=
XM_011522381.2:c.3642-335C= XP_011520683.1:n.3642-335C=
XM_017022944.1:c.4389-335C= XP_016878433.1:n.4389-335C=
NM_004380.3:c.4395-335C= MANE Select NP_004371.2:n.4395-335C=