Canonical Allele Identifier: CA493277628

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3860694G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3810693G>T , CM000678.2:g.3810693G>T	GRCh38
NC_000016.9:g.3860694G>T , CM000678.1:g.3860694G>T	GRCh37
NC_000016.8:g.3800695G>T	NCBI36
NG_009873.1:g.74428C>A
NG_009873.2:g.75021C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.885C>A MANE Select	ENSP00000262367.5:p.Pro295=
ENST00000262367.9:c.885C>A	ENSP00000262367.5:p.Pro295=
ENST00000382070.7:c.885C>A	ENSP00000371502.3:p.Pro295=
NM_001079846.1:c.885C>A	NP_001073315.1:p.Pro295=
NM_004380.2:c.885C>A	NP_004371.2:p.Pro295=
XM_005255124.3:c.885C>A	XP_005255181.1:p.Pro295=
XM_005255125.3:c.885C>A	XP_005255182.1:p.Pro295=
XM_006720848.2:c.885C>A	XP_006720911.1:p.Pro295=
XM_011522380.1:c.831C>A	XP_011520682.1:p.Pro277=
XM_011522381.1:c.132C>A	XP_011520683.1:p.Pro44=
XM_011522382.1:c.885C>A	XP_011520684.1:p.Pro295=
XM_005255124.4:c.885C>A	XP_005255181.1:p.Pro295=
XM_005255125.4:c.885C>A	XP_005255182.1:p.Pro295=
XM_006720848.3:c.885C>A	XP_006720911.1:p.Pro295=
XM_011522381.2:c.132C>A	XP_011520683.1:p.Pro44=
XM_011522382.3:c.885C>A	XP_011520684.1:p.Pro295=
XM_017022944.1:c.885C>A	XP_016878433.1:p.Pro295=
NM_004380.3:c.885C>A MANE Select	NP_004371.2:p.Pro295=