Canonical Allele Identifier: CA2202950925
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3770857C= , CM000678.2:g.3770857C= GRCh38
NC_000016.9:g.3820858C= , CM000678.1:g.3820858C= GRCh37
NC_000016.8:g.3760859C= NCBI36
NG_009873.1:g.114264G=
NG_009873.2:g.114857G=

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.2593G= MANE Select ENSP00000262367.5:p.Gly865=
ENST00000262367.9:c.2593G= ENSP00000262367.5:p.Gly865=
ENST00000382070.7:c.2479G= ENSP00000371502.3:p.Gly827=
ENST00000570939.2:c.1198G= ENSP00000461002.2:p.Gly400=
NM_001079846.1:c.2479G= NP_001073315.1:p.Gly827=
NM_004380.2:c.2593G= NP_004371.2:p.Gly865=
XM_005255124.3:c.2548G= XP_005255181.1:p.Gly850=
XM_005255125.3:c.2464-1504G= XP_005255182.1:n.2464-1504G=
XM_006720848.2:c.2593G= XP_006720911.1:p.Gly865=
XM_011522380.1:c.2539G= XP_011520682.1:p.Gly847=
XM_011522381.1:c.1840G= XP_011520683.1:p.Gly614=
XM_011522382.1:c.2593G= XP_011520684.1:p.Gly865=
XM_005255124.4:c.2548G= XP_005255181.1:p.Gly850=
XM_005255125.4:c.2464-1504G= XP_005255182.1:n.2464-1504G=
XM_006720848.3:c.2593G= XP_006720911.1:p.Gly865=
XM_011522381.2:c.1840G= XP_011520683.1:p.Gly614=
XM_011522382.3:c.2593G= XP_011520684.1:p.Gly865=
XM_017022944.1:c.2587G= XP_016878433.1:p.Gly863=
NM_004380.3:c.2593G= MANE Select NP_004371.2:p.Gly865=