Canonical Allele Identifier: CA394557292
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs2151311904

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3729751C>T , CM000678.2:g.3729751C>T GRCh38
NC_000016.9:g.3779752C>T , CM000678.1:g.3779752C>T GRCh37
NC_000016.8:g.3719753C>T NCBI36
NG_009873.1:g.155370G>A
NG_009873.2:g.155963G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.5296G>A MANE Select ENSP00000262367.5:p.Glu1766Lys
ENST00000262367.9:c.5296G>A ENSP00000262367.5:p.Glu1766Lys
ENST00000382070.7:c.5182G>A ENSP00000371502.3:p.Glu1728Lys
NM_001079846.1:c.5182G>A NP_001073315.1:p.Glu1728Lys
NM_004380.2:c.5296G>A NP_004371.2:p.Glu1766Lys
XM_005255124.3:c.5251G>A XP_005255181.1:p.Glu1751Lys
XM_005255125.3:c.4879G>A XP_005255182.1:p.Glu1627Lys
XM_006720848.2:c.5035G>A XP_006720911.1:p.Glu1679Lys
XM_011522380.1:c.5242G>A XP_011520682.1:p.Glu1748Lys
XM_011522381.1:c.4543G>A XP_011520683.1:p.Glu1515Lys
XM_005255124.4:c.5251G>A XP_005255181.1:p.Glu1751Lys
XM_005255125.4:c.4879G>A XP_005255182.1:p.Glu1627Lys
XM_006720848.3:c.5035G>A XP_006720911.1:p.Glu1679Lys
XM_011522381.2:c.4543G>A XP_011520683.1:p.Glu1515Lys
XM_017022944.1:c.5290G>A XP_016878433.1:p.Glu1764Lys
NM_004380.3:c.5296G>A MANE Select NP_004371.2:p.Glu1766Lys