Canonical Allele Identifier: CA394550147

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151298025
• COSMIC: COSM4060689
• MyVariant Identifiers: chr16:g.3777763C>T (hg19) ; chr16:g.3727762C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727762C>T , CM000678.2:g.3727762C>T	GRCh38
NC_000016.9:g.3777763C>T , CM000678.1:g.3777763C>T	GRCh37
NC_000016.8:g.3717764C>T	NCBI36
NG_009873.1:g.157359G>A
NG_009873.2:g.157952G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7285G>A MANE Select	ENSP00000262367.5:p.Asp2429Asn
ENST00000262367.9:c.7285G>A	ENSP00000262367.5:p.Asp2429Asn
ENST00000382070.7:c.7171G>A	ENSP00000371502.3:p.Asp2391Asn
NM_001079846.1:c.7171G>A	NP_001073315.1:p.Asp2391Asn
NM_004380.2:c.7285G>A	NP_004371.2:p.Asp2429Asn
XM_005255124.3:c.7240G>A	XP_005255181.1:p.Asp2414Asn
XM_005255125.3:c.6868G>A	XP_005255182.1:p.Asp2290Asn
XM_006720848.2:c.7024G>A	XP_006720911.1:p.Asp2342Asn
XM_011522380.1:c.7231G>A	XP_011520682.1:p.Asp2411Asn
XM_011522381.1:c.6532G>A	XP_011520683.1:p.Asp2178Asn
XM_005255124.4:c.7240G>A	XP_005255181.1:p.Asp2414Asn
XM_005255125.4:c.6868G>A	XP_005255182.1:p.Asp2290Asn
XM_006720848.3:c.7024G>A	XP_006720911.1:p.Asp2342Asn
XM_011522381.2:c.6532G>A	XP_011520683.1:p.Asp2178Asn
XM_017022944.1:c.7279G>A	XP_016878433.1:p.Asp2427Asn
NM_004380.3:c.7285G>A MANE Select	NP_004371.2:p.Asp2429Asn