Canonical Allele Identifier: CA394556390

Gene: CREBBP

Linked Data

• dbSNP Id: rs372253007
• MyVariant Identifiers: chr16:g.3779609G>T (hg19) ; chr16:g.3729608G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729608G>T , CM000678.2:g.3729608G>T	GRCh38
NC_000016.9:g.3779609G>T , CM000678.1:g.3779609G>T	GRCh37
NC_000016.8:g.3719610G>T	NCBI36
NG_009873.1:g.155513C>A
NG_009873.2:g.156106C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5439C>A MANE Select	ENSP00000262367.5:p.Asn1813Lys
ENST00000262367.9:c.5439C>A	ENSP00000262367.5:p.Asn1813Lys
ENST00000382070.7:c.5325C>A	ENSP00000371502.3:p.Asn1775Lys
NM_001079846.1:c.5325C>A	NP_001073315.1:p.Asn1775Lys
NM_004380.2:c.5439C>A	NP_004371.2:p.Asn1813Lys
XM_005255124.3:c.5394C>A	XP_005255181.1:p.Asn1798Lys
XM_005255125.3:c.5022C>A	XP_005255182.1:p.Asn1674Lys
XM_006720848.2:c.5178C>A	XP_006720911.1:p.Asn1726Lys
XM_011522380.1:c.5385C>A	XP_011520682.1:p.Asn1795Lys
XM_011522381.1:c.4686C>A	XP_011520683.1:p.Asn1562Lys
XM_005255124.4:c.5394C>A	XP_005255181.1:p.Asn1798Lys
XM_005255125.4:c.5022C>A	XP_005255182.1:p.Asn1674Lys
XM_006720848.3:c.5178C>A	XP_006720911.1:p.Asn1726Lys
XM_011522381.2:c.4686C>A	XP_011520683.1:p.Asn1562Lys
XM_017022944.1:c.5433C>A	XP_016878433.1:p.Asn1811Lys
NM_004380.3:c.5439C>A MANE Select	NP_004371.2:p.Asn1813Lys