Canonical Allele Identifier: CA493394176

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3779690G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729689G>C , CM000678.2:g.3729689G>C	GRCh38
NC_000016.9:g.3779690G>C , CM000678.1:g.3779690G>C	GRCh37
NC_000016.8:g.3719691G>C	NCBI36
NG_009873.1:g.155432C>G
NG_009873.2:g.156025C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5358C>G MANE Select	ENSP00000262367.5:p.Arg1786=
ENST00000262367.9:c.5358C>G	ENSP00000262367.5:p.Arg1786=
ENST00000382070.7:c.5244C>G	ENSP00000371502.3:p.Arg1748=
NM_001079846.1:c.5244C>G	NP_001073315.1:p.Arg1748=
NM_004380.2:c.5358C>G	NP_004371.2:p.Arg1786=
XM_005255124.3:c.5313C>G	XP_005255181.1:p.Arg1771=
XM_005255125.3:c.4941C>G	XP_005255182.1:p.Arg1647=
XM_006720848.2:c.5097C>G	XP_006720911.1:p.Arg1699=
XM_011522380.1:c.5304C>G	XP_011520682.1:p.Arg1768=
XM_011522381.1:c.4605C>G	XP_011520683.1:p.Arg1535=
XM_005255124.4:c.5313C>G	XP_005255181.1:p.Arg1771=
XM_005255125.4:c.4941C>G	XP_005255182.1:p.Arg1647=
XM_006720848.3:c.5097C>G	XP_006720911.1:p.Arg1699=
XM_011522381.2:c.4605C>G	XP_011520683.1:p.Arg1535=
XM_017022944.1:c.5352C>G	XP_016878433.1:p.Arg1784=
NM_004380.3:c.5358C>G MANE Select	NP_004371.2:p.Arg1786=