Canonical Allele Identifier: CA394556228

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151310467
• MyVariant Identifiers: chr16:g.3779568C>A (hg19) ; chr16:g.3729567C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729567C>A , CM000678.2:g.3729567C>A	GRCh38
NC_000016.9:g.3779568C>A , CM000678.1:g.3779568C>A	GRCh37
NC_000016.8:g.3719569C>A	NCBI36
NG_009873.1:g.155554G>T
NG_009873.2:g.156147G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5480G>T MANE Select	ENSP00000262367.5:p.Cys1827Phe
ENST00000262367.9:c.5480G>T	ENSP00000262367.5:p.Cys1827Phe
ENST00000382070.7:c.5366G>T	ENSP00000371502.3:p.Cys1789Phe
NM_001079846.1:c.5366G>T	NP_001073315.1:p.Cys1789Phe
NM_004380.2:c.5480G>T	NP_004371.2:p.Cys1827Phe
XM_005255124.3:c.5435G>T	XP_005255181.1:p.Cys1812Phe
XM_005255125.3:c.5063G>T	XP_005255182.1:p.Cys1688Phe
XM_006720848.2:c.5219G>T	XP_006720911.1:p.Cys1740Phe
XM_011522380.1:c.5426G>T	XP_011520682.1:p.Cys1809Phe
XM_011522381.1:c.4727G>T	XP_011520683.1:p.Cys1576Phe
XM_005255124.4:c.5435G>T	XP_005255181.1:p.Cys1812Phe
XM_005255125.4:c.5063G>T	XP_005255182.1:p.Cys1688Phe
XM_006720848.3:c.5219G>T	XP_006720911.1:p.Cys1740Phe
XM_011522381.2:c.4727G>T	XP_011520683.1:p.Cys1576Phe
XM_017022944.1:c.5474G>T	XP_016878433.1:p.Cys1825Phe
NM_004380.3:c.5480G>T MANE Select	NP_004371.2:p.Cys1827Phe