Canonical Allele Identifier: CA493394087

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3779510G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729509G>T , CM000678.2:g.3729509G>T	GRCh38
NC_000016.9:g.3779510G>T , CM000678.1:g.3779510G>T	GRCh37
NC_000016.8:g.3719511G>T	NCBI36
NG_009873.1:g.155612C>A
NG_009873.2:g.156205C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5538C>A MANE Select	ENSP00000262367.5:p.Ile1846=
ENST00000262367.9:c.5538C>A	ENSP00000262367.5:p.Ile1846=
ENST00000382070.7:c.5424C>A	ENSP00000371502.3:p.Ile1808=
NM_001079846.1:c.5424C>A	NP_001073315.1:p.Ile1808=
NM_004380.2:c.5538C>A	NP_004371.2:p.Ile1846=
XM_005255124.3:c.5493C>A	XP_005255181.1:p.Ile1831=
XM_005255125.3:c.5121C>A	XP_005255182.1:p.Ile1707=
XM_006720848.2:c.5277C>A	XP_006720911.1:p.Ile1759=
XM_011522380.1:c.5484C>A	XP_011520682.1:p.Ile1828=
XM_011522381.1:c.4785C>A	XP_011520683.1:p.Ile1595=
XM_005255124.4:c.5493C>A	XP_005255181.1:p.Ile1831=
XM_005255125.4:c.5121C>A	XP_005255182.1:p.Ile1707=
XM_006720848.3:c.5277C>A	XP_006720911.1:p.Ile1759=
XM_011522381.2:c.4785C>A	XP_011520683.1:p.Ile1595=
XM_017022944.1:c.5532C>A	XP_016878433.1:p.Ile1844=
NM_004380.3:c.5538C>A MANE Select	NP_004371.2:p.Ile1846=