Canonical Allele Identifier: CA394551100

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3778098T>G (hg19) ; chr16:g.3728097T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728097T>G , CM000678.2:g.3728097T>G	GRCh38
NC_000016.9:g.3778098T>G , CM000678.1:g.3778098T>G	GRCh37
NC_000016.8:g.3718099T>G	NCBI36
NG_009873.1:g.157024A>C
NG_009873.2:g.157617A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6950A>C MANE Select	ENSP00000262367.5:p.Gln2317Pro
ENST00000262367.9:c.6950A>C	ENSP00000262367.5:p.Gln2317Pro
ENST00000382070.7:c.6836A>C	ENSP00000371502.3:p.Gln2279Pro
NM_001079846.1:c.6836A>C	NP_001073315.1:p.Gln2279Pro
NM_004380.2:c.6950A>C	NP_004371.2:p.Gln2317Pro
XM_005255124.3:c.6905A>C	XP_005255181.1:p.Gln2302Pro
XM_005255125.3:c.6533A>C	XP_005255182.1:p.Gln2178Pro
XM_006720848.2:c.6689A>C	XP_006720911.1:p.Gln2230Pro
XM_011522380.1:c.6896A>C	XP_011520682.1:p.Gln2299Pro
XM_011522381.1:c.6197A>C	XP_011520683.1:p.Gln2066Pro
XM_005255124.4:c.6905A>C	XP_005255181.1:p.Gln2302Pro
XM_005255125.4:c.6533A>C	XP_005255182.1:p.Gln2178Pro
XM_006720848.3:c.6689A>C	XP_006720911.1:p.Gln2230Pro
XM_011522381.2:c.6197A>C	XP_011520683.1:p.Gln2066Pro
XM_017022944.1:c.6944A>C	XP_016878433.1:p.Gln2315Pro
NM_004380.3:c.6950A>C MANE Select	NP_004371.2:p.Gln2317Pro