Canonical Allele Identifier: CA493279678

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151330143
• MyVariant Identifiers: chr16:g.3786807T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3736806T>C , CM000678.2:g.3736806T>C	GRCh38
NC_000016.9:g.3786807T>C , CM000678.1:g.3786807T>C	GRCh37
NC_000016.8:g.3726808T>C	NCBI36
NG_009873.1:g.148315A>G
NG_009873.2:g.148908A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.4404A>G MANE Select	ENSP00000262367.5:p.Thr1468=
ENST00000262367.9:c.4404A>G	ENSP00000262367.5:p.Thr1468=
ENST00000382070.7:c.4290A>G	ENSP00000371502.3:p.Thr1430=
ENST00000570939.2:c.3039A>G	ENSP00000461002.2:p.Thr1013=
ENST00000571763.5:n.194A>G
ENST00000574740.1:n.225A>G
ENST00000576720.1:n.3227A>G
NM_001079846.1:c.4290A>G	NP_001073315.1:p.Thr1430=
NM_004380.2:c.4404A>G	NP_004371.2:p.Thr1468=
XM_005255124.3:c.4359A>G	XP_005255181.1:p.Thr1453=
XM_005255125.3:c.3987A>G	XP_005255182.1:p.Thr1329=
XM_006720848.2:c.4143A>G	XP_006720911.1:p.Thr1381=
XM_011522380.1:c.4350A>G	XP_011520682.1:p.Thr1450=
XM_011522381.1:c.3651A>G	XP_011520683.1:p.Thr1217=
XM_005255124.4:c.4359A>G	XP_005255181.1:p.Thr1453=
XM_005255125.4:c.3987A>G	XP_005255182.1:p.Thr1329=
XM_006720848.3:c.4143A>G	XP_006720911.1:p.Thr1381=
XM_011522381.2:c.3651A>G	XP_011520683.1:p.Thr1217=
XM_017022944.1:c.4398A>G	XP_016878433.1:p.Thr1466=
NM_004380.3:c.4404A>G MANE Select	NP_004371.2:p.Thr1468=