Canonical Allele Identifier: CA394550090

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151297872
• MyVariant Identifiers: chr16:g.3777736A>T (hg19) ; chr16:g.3727735A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727735A>T , CM000678.2:g.3727735A>T	GRCh38
NC_000016.9:g.3777736A>T , CM000678.1:g.3777736A>T	GRCh37
NC_000016.8:g.3717737A>T	NCBI36
NG_009873.1:g.157386T>A
NG_009873.2:g.157979T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7312T>A MANE Select	ENSP00000262367.5:p.Phe2438Ile
ENST00000262367.9:c.7312T>A	ENSP00000262367.5:p.Phe2438Ile
ENST00000382070.7:c.7198T>A	ENSP00000371502.3:p.Phe2400Ile
NM_001079846.1:c.7198T>A	NP_001073315.1:p.Phe2400Ile
NM_004380.2:c.7312T>A	NP_004371.2:p.Phe2438Ile
XM_005255124.3:c.7267T>A	XP_005255181.1:p.Phe2423Ile
XM_005255125.3:c.6895T>A	XP_005255182.1:p.Phe2299Ile
XM_006720848.2:c.7051T>A	XP_006720911.1:p.Phe2351Ile
XM_011522380.1:c.7258T>A	XP_011520682.1:p.Phe2420Ile
XM_011522381.1:c.6559T>A	XP_011520683.1:p.Phe2187Ile
XM_005255124.4:c.7267T>A	XP_005255181.1:p.Phe2423Ile
XM_005255125.4:c.6895T>A	XP_005255182.1:p.Phe2299Ile
XM_006720848.3:c.7051T>A	XP_006720911.1:p.Phe2351Ile
XM_011522381.2:c.6559T>A	XP_011520683.1:p.Phe2187Ile
XM_017022944.1:c.7306T>A	XP_016878433.1:p.Phe2436Ile
NM_004380.3:c.7312T>A MANE Select	NP_004371.2:p.Phe2438Ile