Canonical Allele Identifier: CA394563873

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3786757T>C (hg19) ; chr16:g.3736756T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3736756T>C , CM000678.2:g.3736756T>C	GRCh38
NC_000016.9:g.3786757T>C , CM000678.1:g.3786757T>C	GRCh37
NC_000016.8:g.3726758T>C	NCBI36
NG_009873.1:g.148365A>G
NG_009873.2:g.148958A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.4454A>G MANE Select	ENSP00000262367.5:p.His1485Arg
ENST00000262367.9:c.4454A>G	ENSP00000262367.5:p.His1485Arg
ENST00000382070.7:c.4340A>G	ENSP00000371502.3:p.His1447Arg
ENST00000570939.2:c.3089A>G	ENSP00000461002.2:p.His1030Arg
ENST00000571763.5:n.244A>G
ENST00000574740.1:n.275A>G
ENST00000576720.1:n.3277A>G
NM_001079846.1:c.4340A>G	NP_001073315.1:p.His1447Arg
NM_004380.2:c.4454A>G	NP_004371.2:p.His1485Arg
XM_005255124.3:c.4409A>G	XP_005255181.1:p.His1470Arg
XM_005255125.3:c.4037A>G	XP_005255182.1:p.His1346Arg
XM_006720848.2:c.4193A>G	XP_006720911.1:p.His1398Arg
XM_011522380.1:c.4400A>G	XP_011520682.1:p.His1467Arg
XM_011522381.1:c.3701A>G	XP_011520683.1:p.His1234Arg
XM_005255124.4:c.4409A>G	XP_005255181.1:p.His1470Arg
XM_005255125.4:c.4037A>G	XP_005255182.1:p.His1346Arg
XM_006720848.3:c.4193A>G	XP_006720911.1:p.His1398Arg
XM_011522381.2:c.3701A>G	XP_011520683.1:p.His1234Arg
XM_017022944.1:c.4448A>G	XP_016878433.1:p.His1483Arg
NM_004380.3:c.4454A>G MANE Select	NP_004371.2:p.His1485Arg