Canonical Allele Identifier: CA394563286

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151329130
• MyVariant Identifiers: chr16:g.3786659C>A (hg19) ; chr16:g.3736658C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3736658C>A , CM000678.2:g.3736658C>A	GRCh38
NC_000016.9:g.3786659C>A , CM000678.1:g.3786659C>A	GRCh37
NC_000016.8:g.3726660C>A	NCBI36
NG_009873.1:g.148463G>T
NG_009873.2:g.149056G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.4552G>T MANE Select	ENSP00000262367.5:p.Asp1518Tyr
ENST00000262367.9:c.4552G>T	ENSP00000262367.5:p.Asp1518Tyr
ENST00000382070.7:c.4438G>T	ENSP00000371502.3:p.Asp1480Tyr
ENST00000570939.2:c.3187G>T	ENSP00000461002.2:p.Asp1063Tyr
ENST00000571763.5:n.342G>T
ENST00000574740.1:n.373G>T
ENST00000576720.1:n.3375G>T
NM_001079846.1:c.4438G>T	NP_001073315.1:p.Asp1480Tyr
NM_004380.2:c.4552G>T	NP_004371.2:p.Asp1518Tyr
XM_005255124.3:c.4507G>T	XP_005255181.1:p.Asp1503Tyr
XM_005255125.3:c.4135G>T	XP_005255182.1:p.Asp1379Tyr
XM_006720848.2:c.4291G>T	XP_006720911.1:p.Asp1431Tyr
XM_011522380.1:c.4498G>T	XP_011520682.1:p.Asp1500Tyr
XM_011522381.1:c.3799G>T	XP_011520683.1:p.Asp1267Tyr
XM_005255124.4:c.4507G>T	XP_005255181.1:p.Asp1503Tyr
XM_005255125.4:c.4135G>T	XP_005255182.1:p.Asp1379Tyr
XM_006720848.3:c.4291G>T	XP_006720911.1:p.Asp1431Tyr
XM_011522381.2:c.3799G>T	XP_011520683.1:p.Asp1267Tyr
XM_017022944.1:c.4546G>T	XP_016878433.1:p.Asp1516Tyr
NM_004380.3:c.4552G>T MANE Select	NP_004371.2:p.Asp1518Tyr