Canonical Allele Identifier: CA394562228

Gene: CREBBP

Linked Data

• dbSNP Id: rs2141285208
• MyVariant Identifiers: chr16:g.3843405C>T (hg19) ; chr16:g.3793404C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3793404C>T , CM000678.2:g.3793404C>T	GRCh38
NC_000016.9:g.3843405C>T , CM000678.1:g.3843405C>T	GRCh37
NC_000016.8:g.3783406C>T	NCBI36
NG_009873.1:g.91717G>A
NG_009873.2:g.92310G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000262367.10:c.1198G>A MANE Select	ENSP00000262367.5:p.Ala400Thr
ENST00000262367.9:c.1198G>A	ENSP00000262367.5:p.Ala400Thr
ENST00000382070.7:c.1198G>A	ENSP00000371502.3:p.Ala400Thr
NM_001079846.1:c.1198G>A	NP_001073315.1:p.Ala400Thr
NM_004380.2:c.1198G>A	NP_004371.2:p.Ala400Thr
XM_005255124.3:c.1198G>A	XP_005255181.1:p.Ala400Thr
XM_005255125.3:c.1198G>A	XP_005255182.1:p.Ala400Thr
XM_006720848.2:c.1198G>A	XP_006720911.1:p.Ala400Thr
XM_011522380.1:c.1144G>A	XP_011520682.1:p.Ala382Thr
XM_011522381.1:c.445G>A	XP_011520683.1:p.Ala149Thr
XM_011522382.1:c.1198G>A	XP_011520684.1:p.Ala400Thr
XM_005255124.4:c.1198G>A	XP_005255181.1:p.Ala400Thr
XM_005255125.4:c.1198G>A	XP_005255182.1:p.Ala400Thr
XM_006720848.3:c.1198G>A	XP_006720911.1:p.Ala400Thr
XM_011522381.2:c.445G>A	XP_011520683.1:p.Ala149Thr
XM_011522382.3:c.1198G>A	XP_011520684.1:p.Ala400Thr
XM_017022944.1:c.1198G>A	XP_016878433.1:p.Ala400Thr
NM_004380.3:c.1198G>A MANE Select	NP_004371.2:p.Ala400Thr