Canonical Allele Identifier: CA394550301

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151298550
• MyVariant Identifiers: chr16:g.3777837T>G (hg19) ; chr16:g.3727836T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727836T>G , CM000678.2:g.3727836T>G	GRCh38
NC_000016.9:g.3777837T>G , CM000678.1:g.3777837T>G	GRCh37
NC_000016.8:g.3717838T>G	NCBI36
NG_009873.1:g.157285A>C
NG_009873.2:g.157878A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7211A>C MANE Select	ENSP00000262367.5:p.Glu2404Ala
ENST00000262367.9:c.7211A>C	ENSP00000262367.5:p.Glu2404Ala
ENST00000382070.7:c.7097A>C	ENSP00000371502.3:p.Glu2366Ala
NM_001079846.1:c.7097A>C	NP_001073315.1:p.Glu2366Ala
NM_004380.2:c.7211A>C	NP_004371.2:p.Glu2404Ala
XM_005255124.3:c.7166A>C	XP_005255181.1:p.Glu2389Ala
XM_005255125.3:c.6794A>C	XP_005255182.1:p.Glu2265Ala
XM_006720848.2:c.6950A>C	XP_006720911.1:p.Glu2317Ala
XM_011522380.1:c.7157A>C	XP_011520682.1:p.Glu2386Ala
XM_011522381.1:c.6458A>C	XP_011520683.1:p.Glu2153Ala
XM_005255124.4:c.7166A>C	XP_005255181.1:p.Glu2389Ala
XM_005255125.4:c.6794A>C	XP_005255182.1:p.Glu2265Ala
XM_006720848.3:c.6950A>C	XP_006720911.1:p.Glu2317Ala
XM_011522381.2:c.6458A>C	XP_011520683.1:p.Glu2153Ala
XM_017022944.1:c.7205A>C	XP_016878433.1:p.Glu2402Ala
NM_004380.3:c.7211A>C MANE Select	NP_004371.2:p.Glu2404Ala