Canonical Allele Identifier: CA493394378

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3779624G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729623G>A , CM000678.2:g.3729623G>A	GRCh38
NC_000016.9:g.3779624G>A , CM000678.1:g.3779624G>A	GRCh37
NC_000016.8:g.3719625G>A	NCBI36
NG_009873.1:g.155498C>T
NG_009873.2:g.156091C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5424C>T MANE Select	ENSP00000262367.5:p.Cys1808=
ENST00000262367.9:c.5424C>T	ENSP00000262367.5:p.Cys1808=
ENST00000382070.7:c.5310C>T	ENSP00000371502.3:p.Cys1770=
NM_001079846.1:c.5310C>T	NP_001073315.1:p.Cys1770=
NM_004380.2:c.5424C>T	NP_004371.2:p.Cys1808=
XM_005255124.3:c.5379C>T	XP_005255181.1:p.Cys1793=
XM_005255125.3:c.5007C>T	XP_005255182.1:p.Cys1669=
XM_006720848.2:c.5163C>T	XP_006720911.1:p.Cys1721=
XM_011522380.1:c.5370C>T	XP_011520682.1:p.Cys1790=
XM_011522381.1:c.4671C>T	XP_011520683.1:p.Cys1557=
XM_005255124.4:c.5379C>T	XP_005255181.1:p.Cys1793=
XM_005255125.4:c.5007C>T	XP_005255182.1:p.Cys1669=
XM_006720848.3:c.5163C>T	XP_006720911.1:p.Cys1721=
XM_011522381.2:c.4671C>T	XP_011520683.1:p.Cys1557=
XM_017022944.1:c.5418C>T	XP_016878433.1:p.Cys1806=
NM_004380.3:c.5424C>T MANE Select	NP_004371.2:p.Cys1808=