Canonical Allele Identifier: CA2202937011
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3737064A= , CM000678.2:g.3737064A= GRCh38
NC_000016.9:g.3787065A= , CM000678.1:g.3787065A= GRCh37
NC_000016.8:g.3727066A= NCBI36
NG_009873.1:g.148057T=
NG_009873.2:g.148650T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.4395-249T= MANE Select ENSP00000262367.5:n.4395-249T=
ENST00000262367.9:c.4395-249T= ENSP00000262367.5:n.4395-249T=
ENST00000382070.7:c.4281-249T= ENSP00000371502.3:n.4281-249T=
ENST00000570939.2:c.3030-249T= ENSP00000461002.2:n.3030-249T=
ENST00000574740.1:n.216-249T=
ENST00000576720.1:n.3218-249T=
NM_001079846.1:c.4281-249T= NP_001073315.1:n.4281-249T=
NM_004380.2:c.4395-249T= NP_004371.2:n.4395-249T=
XM_005255124.3:c.4350-249T= XP_005255181.1:n.4350-249T=
XM_005255125.3:c.3978-249T= XP_005255182.1:n.3978-249T=
XM_006720848.2:c.4134-249T= XP_006720911.1:n.4134-249T=
XM_011522380.1:c.4341-249T= XP_011520682.1:n.4341-249T=
XM_011522381.1:c.3642-249T= XP_011520683.1:n.3642-249T=
XM_005255124.4:c.4350-249T= XP_005255181.1:n.4350-249T=
XM_005255125.4:c.3978-249T= XP_005255182.1:n.3978-249T=
XM_006720848.3:c.4134-249T= XP_006720911.1:n.4134-249T=
XM_011522381.2:c.3642-249T= XP_011520683.1:n.3642-249T=
XM_017022944.1:c.4389-249T= XP_016878433.1:n.4389-249T=
NM_004380.3:c.4395-249T= MANE Select NP_004371.2:n.4395-249T=