Canonical Allele Identifier: CA394563587

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3786709T>G (hg19) ; chr16:g.3736708T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3736708T>G , CM000678.2:g.3736708T>G	GRCh38
NC_000016.9:g.3786709T>G , CM000678.1:g.3786709T>G	GRCh37
NC_000016.8:g.3726710T>G	NCBI36
NG_009873.1:g.148413A>C
NG_009873.2:g.149006A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.4502A>C MANE Select	ENSP00000262367.5:p.Glu1501Ala
ENST00000262367.9:c.4502A>C	ENSP00000262367.5:p.Glu1501Ala
ENST00000382070.7:c.4388A>C	ENSP00000371502.3:p.Glu1463Ala
ENST00000570939.2:c.3137A>C	ENSP00000461002.2:p.Glu1046Ala
ENST00000571763.5:n.292A>C
ENST00000574740.1:n.323A>C
ENST00000576720.1:n.3325A>C
NM_001079846.1:c.4388A>C	NP_001073315.1:p.Glu1463Ala
NM_004380.2:c.4502A>C	NP_004371.2:p.Glu1501Ala
XM_005255124.3:c.4457A>C	XP_005255181.1:p.Glu1486Ala
XM_005255125.3:c.4085A>C	XP_005255182.1:p.Glu1362Ala
XM_006720848.2:c.4241A>C	XP_006720911.1:p.Glu1414Ala
XM_011522380.1:c.4448A>C	XP_011520682.1:p.Glu1483Ala
XM_011522381.1:c.3749A>C	XP_011520683.1:p.Glu1250Ala
XM_005255124.4:c.4457A>C	XP_005255181.1:p.Glu1486Ala
XM_005255125.4:c.4085A>C	XP_005255182.1:p.Glu1362Ala
XM_006720848.3:c.4241A>C	XP_006720911.1:p.Glu1414Ala
XM_011522381.2:c.3749A>C	XP_011520683.1:p.Glu1250Ala
XM_017022944.1:c.4496A>C	XP_016878433.1:p.Glu1499Ala
NM_004380.3:c.4502A>C MANE Select	NP_004371.2:p.Glu1501Ala