Canonical Allele Identifier: CA493279470

Gene: CREBBP

Linked Data

• COSMIC: COSM1128960
• MyVariant Identifiers: chr16:g.3786756A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3736755A>G , CM000678.2:g.3736755A>G	GRCh38
NC_000016.9:g.3786756A>G , CM000678.1:g.3786756A>G	GRCh37
NC_000016.8:g.3726757A>G	NCBI36
NG_009873.1:g.148366T>C
NG_009873.2:g.148959T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.4455T>C MANE Select	ENSP00000262367.5:p.His1485=
ENST00000262367.9:c.4455T>C	ENSP00000262367.5:p.His1485=
ENST00000382070.7:c.4341T>C	ENSP00000371502.3:p.His1447=
ENST00000570939.2:c.3090T>C	ENSP00000461002.2:p.His1030=
ENST00000571763.5:n.245T>C
ENST00000574740.1:n.276T>C
ENST00000576720.1:n.3278T>C
NM_001079846.1:c.4341T>C	NP_001073315.1:p.His1447=
NM_004380.2:c.4455T>C	NP_004371.2:p.His1485=
XM_005255124.3:c.4410T>C	XP_005255181.1:p.His1470=
XM_005255125.3:c.4038T>C	XP_005255182.1:p.His1346=
XM_006720848.2:c.4194T>C	XP_006720911.1:p.His1398=
XM_011522380.1:c.4401T>C	XP_011520682.1:p.His1467=
XM_011522381.1:c.3702T>C	XP_011520683.1:p.His1234=
XM_005255124.4:c.4410T>C	XP_005255181.1:p.His1470=
XM_005255125.4:c.4038T>C	XP_005255182.1:p.His1346=
XM_006720848.3:c.4194T>C	XP_006720911.1:p.His1398=
XM_011522381.2:c.3702T>C	XP_011520683.1:p.His1234=
XM_017022944.1:c.4449T>C	XP_016878433.1:p.His1483=
NM_004380.3:c.4455T>C MANE Select	NP_004371.2:p.His1485=