Canonical Allele Identifier: CA394553695

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3778750A>C (hg19) ; chr16:g.3728749A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728749A>C , CM000678.2:g.3728749A>C	GRCh38
NC_000016.9:g.3778750A>C , CM000678.1:g.3778750A>C	GRCh37
NC_000016.8:g.3718751A>C	NCBI36
NG_009873.1:g.156372T>G
NG_009873.2:g.156965T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6298T>G MANE Select	ENSP00000262367.5:p.Phe2100Val
ENST00000262367.9:c.6298T>G	ENSP00000262367.5:p.Phe2100Val
ENST00000382070.7:c.6184T>G	ENSP00000371502.3:p.Phe2062Val
NM_001079846.1:c.6184T>G	NP_001073315.1:p.Phe2062Val
NM_004380.2:c.6298T>G	NP_004371.2:p.Phe2100Val
XM_005255124.3:c.6253T>G	XP_005255181.1:p.Phe2085Val
XM_005255125.3:c.5881T>G	XP_005255182.1:p.Phe1961Val
XM_006720848.2:c.6037T>G	XP_006720911.1:p.Phe2013Val
XM_011522380.1:c.6244T>G	XP_011520682.1:p.Phe2082Val
XM_011522381.1:c.5545T>G	XP_011520683.1:p.Phe1849Val
XM_005255124.4:c.6253T>G	XP_005255181.1:p.Phe2085Val
XM_005255125.4:c.5881T>G	XP_005255182.1:p.Phe1961Val
XM_006720848.3:c.6037T>G	XP_006720911.1:p.Phe2013Val
XM_011522381.2:c.5545T>G	XP_011520683.1:p.Phe1849Val
XM_017022944.1:c.6292T>G	XP_016878433.1:p.Phe2098Val
NM_004380.3:c.6298T>G MANE Select	NP_004371.2:p.Phe2100Val