Canonical Allele Identifier: CA394556399

Gene: CREBBP

Linked Data

• dbSNP Id: rs1443048838
• MyVariant Identifiers: chr16:g.3779610T>G (hg19) ; chr16:g.3729609T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729609T>G , CM000678.2:g.3729609T>G	GRCh38
NC_000016.9:g.3779610T>G , CM000678.1:g.3779610T>G	GRCh37
NC_000016.8:g.3719611T>G	NCBI36
NG_009873.1:g.155512A>C
NG_009873.2:g.156105A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5438A>C MANE Select	ENSP00000262367.5:p.Asn1813Thr
ENST00000262367.9:c.5438A>C	ENSP00000262367.5:p.Asn1813Thr
ENST00000382070.7:c.5324A>C	ENSP00000371502.3:p.Asn1775Thr
NM_001079846.1:c.5324A>C	NP_001073315.1:p.Asn1775Thr
NM_004380.2:c.5438A>C	NP_004371.2:p.Asn1813Thr
XM_005255124.3:c.5393A>C	XP_005255181.1:p.Asn1798Thr
XM_005255125.3:c.5021A>C	XP_005255182.1:p.Asn1674Thr
XM_006720848.2:c.5177A>C	XP_006720911.1:p.Asn1726Thr
XM_011522380.1:c.5384A>C	XP_011520682.1:p.Asn1795Thr
XM_011522381.1:c.4685A>C	XP_011520683.1:p.Asn1562Thr
XM_005255124.4:c.5393A>C	XP_005255181.1:p.Asn1798Thr
XM_005255125.4:c.5021A>C	XP_005255182.1:p.Asn1674Thr
XM_006720848.3:c.5177A>C	XP_006720911.1:p.Asn1726Thr
XM_011522381.2:c.4685A>C	XP_011520683.1:p.Asn1562Thr
XM_017022944.1:c.5432A>C	XP_016878433.1:p.Asn1811Thr
NM_004380.3:c.5438A>C MANE Select	NP_004371.2:p.Asn1813Thr