Canonical Allele Identifier: CA394558006

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3731196C>A , CM000678.2:g.3731196C>A	GRCh38
NC_000016.9:g.3781197C>A , CM000678.1:g.3781197C>A	GRCh37
NC_000016.8:g.3721198C>A	NCBI36
NG_009873.1:g.153925G>T
NG_009873.2:g.154518G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004380.3:c.5168G>T MANE Select	NP_004371.2:p.Cys1723Phe
ENST00000262367.10:c.5168G>T MANE Select	ENSP00000262367.5:p.Cys1723Phe
NM_001079846.1:c.5054G>T	NP_001073315.1:p.Cys1685Phe
NM_004380.2:c.5168G>T	NP_004371.2:p.Cys1723Phe
ENST00000262367.9:c.5168G>T	ENSP00000262367.5:p.Cys1723Phe
ENST00000382070.7:c.5054G>T	ENSP00000371502.3:p.Cys1685Phe
ENST00000637492.1:c.55G>T
XM_005255124.3:c.5123G>T	XP_005255181.1:p.Cys1708Phe
XM_005255124.4:c.5123G>T	XP_005255181.1:p.Cys1708Phe
XM_005255125.3:c.4751G>T	XP_005255182.1:p.Cys1584Phe
XM_005255125.4:c.4751G>T	XP_005255182.1:p.Cys1584Phe
XM_006720848.2:c.4907G>T	XP_006720911.1:p.Cys1636Phe
XM_006720848.3:c.4907G>T	XP_006720911.1:p.Cys1636Phe
XM_011522380.1:c.5114G>T	XP_011520682.1:p.Cys1705Phe
XM_011522381.1:c.4415G>T	XP_011520683.1:p.Cys1472Phe
XM_011522381.2:c.4415G>T	XP_011520683.1:p.Cys1472Phe
XM_017022944.1:c.5162G>T	XP_016878433.1:p.Cys1721Phe