Canonical Allele Identifier: CA493277681

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3860772T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3810771T>G , CM000678.2:g.3810771T>G	GRCh38
NC_000016.9:g.3860772T>G , CM000678.1:g.3860772T>G	GRCh37
NC_000016.8:g.3800773T>G	NCBI36
NG_009873.1:g.74350A>C
NG_009873.2:g.74943A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.807A>C MANE Select	ENSP00000262367.5:p.Ile269=
ENST00000635899.1:n.49A>C
ENST00000262367.9:c.807A>C	ENSP00000262367.5:p.Ile269=
ENST00000382070.7:c.807A>C	ENSP00000371502.3:p.Ile269=
NM_001079846.1:c.807A>C	NP_001073315.1:p.Ile269=
NM_004380.2:c.807A>C	NP_004371.2:p.Ile269=
XM_005255124.3:c.807A>C	XP_005255181.1:p.Ile269=
XM_005255125.3:c.807A>C	XP_005255182.1:p.Ile269=
XM_006720848.2:c.807A>C	XP_006720911.1:p.Ile269=
XM_011522380.1:c.753A>C	XP_011520682.1:p.Ile251=
XM_011522381.1:c.54A>C	XP_011520683.1:p.Ile18=
XM_011522382.1:c.807A>C	XP_011520684.1:p.Ile269=
XM_005255124.4:c.807A>C	XP_005255181.1:p.Ile269=
XM_005255125.4:c.807A>C	XP_005255182.1:p.Ile269=
XM_006720848.3:c.807A>C	XP_006720911.1:p.Ile269=
XM_011522381.2:c.54A>C	XP_011520683.1:p.Ile18=
XM_011522382.3:c.807A>C	XP_011520684.1:p.Ile269=
XM_017022944.1:c.807A>C	XP_016878433.1:p.Ile269=
NM_004380.3:c.807A>C MANE Select	NP_004371.2:p.Ile269=