Canonical Allele Identifier: CA394556015

Gene: CREBBP

Linked Data

• ClinVar Variation Id: 981358
• ClinVar RCV Id: RCV001260744
• dbSNP Id: rs2051852330
• MyVariant Identifiers: chr16:g.3779487T>G (hg19) ; chr16:g.3729486T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729486T>G , CM000678.2:g.3729486T>G	GRCh38
NC_000016.9:g.3779487T>G , CM000678.1:g.3779487T>G	GRCh37
NC_000016.8:g.3719488T>G	NCBI36
NG_009873.1:g.155635A>C
NG_009873.2:g.156228A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5561A>C MANE Select	ENSP00000262367.5:p.Gln1854Pro
ENST00000262367.9:c.5561A>C	ENSP00000262367.5:p.Gln1854Pro
ENST00000382070.7:c.5447A>C	ENSP00000371502.3:p.Gln1816Pro
NM_001079846.1:c.5447A>C	NP_001073315.1:p.Gln1816Pro
NM_004380.2:c.5561A>C	NP_004371.2:p.Gln1854Pro
XM_005255124.3:c.5516A>C	XP_005255181.1:p.Gln1839Pro
XM_005255125.3:c.5144A>C	XP_005255182.1:p.Gln1715Pro
XM_006720848.2:c.5300A>C	XP_006720911.1:p.Gln1767Pro
XM_011522380.1:c.5507A>C	XP_011520682.1:p.Gln1836Pro
XM_011522381.1:c.4808A>C	XP_011520683.1:p.Gln1603Pro
XM_005255124.4:c.5516A>C	XP_005255181.1:p.Gln1839Pro
XM_005255125.4:c.5144A>C	XP_005255182.1:p.Gln1715Pro
XM_006720848.3:c.5300A>C	XP_006720911.1:p.Gln1767Pro
XM_011522381.2:c.4808A>C	XP_011520683.1:p.Gln1603Pro
XM_017022944.1:c.5555A>C	XP_016878433.1:p.Gln1852Pro
NM_004380.3:c.5561A>C MANE Select	NP_004371.2:p.Gln1854Pro