Canonical Allele Identifier: CA394563887

Gene: CREBBP

Linked Data

• COSMIC: COSM5651302
• MyVariant Identifiers: chr16:g.3786760A>C (hg19) ; chr16:g.3736759A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3736759A>C , CM000678.2:g.3736759A>C	GRCh38
NC_000016.9:g.3786760A>C , CM000678.1:g.3786760A>C	GRCh37
NC_000016.8:g.3726761A>C	NCBI36
NG_009873.1:g.148362T>G
NG_009873.2:g.148955T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.4451T>G MANE Select	ENSP00000262367.5:p.Phe1484Cys
ENST00000262367.9:c.4451T>G	ENSP00000262367.5:p.Phe1484Cys
ENST00000382070.7:c.4337T>G	ENSP00000371502.3:p.Phe1446Cys
ENST00000570939.2:c.3086T>G	ENSP00000461002.2:p.Phe1029Cys
ENST00000571763.5:n.241T>G
ENST00000574740.1:n.272T>G
ENST00000576720.1:n.3274T>G
NM_001079846.1:c.4337T>G	NP_001073315.1:p.Phe1446Cys
NM_004380.2:c.4451T>G	NP_004371.2:p.Phe1484Cys
XM_005255124.3:c.4406T>G	XP_005255181.1:p.Phe1469Cys
XM_005255125.3:c.4034T>G	XP_005255182.1:p.Phe1345Cys
XM_006720848.2:c.4190T>G	XP_006720911.1:p.Phe1397Cys
XM_011522380.1:c.4397T>G	XP_011520682.1:p.Phe1466Cys
XM_011522381.1:c.3698T>G	XP_011520683.1:p.Phe1233Cys
XM_005255124.4:c.4406T>G	XP_005255181.1:p.Phe1469Cys
XM_005255125.4:c.4034T>G	XP_005255182.1:p.Phe1345Cys
XM_006720848.3:c.4190T>G	XP_006720911.1:p.Phe1397Cys
XM_011522381.2:c.3698T>G	XP_011520683.1:p.Phe1233Cys
XM_017022944.1:c.4445T>G	XP_016878433.1:p.Phe1482Cys
NM_004380.3:c.4451T>G MANE Select	NP_004371.2:p.Phe1484Cys