Canonical Allele Identifier: CA394556036

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3779496C>G (hg19) ; chr16:g.3729495C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729495C>G , CM000678.2:g.3729495C>G	GRCh38
NC_000016.9:g.3779496C>G , CM000678.1:g.3779496C>G	GRCh37
NC_000016.8:g.3719497C>G	NCBI36
NG_009873.1:g.155626G>C
NG_009873.2:g.156219G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5552G>C MANE Select	ENSP00000262367.5:p.Arg1851Pro
ENST00000262367.9:c.5552G>C	ENSP00000262367.5:p.Arg1851Pro
ENST00000382070.7:c.5438G>C	ENSP00000371502.3:p.Arg1813Pro
NM_001079846.1:c.5438G>C	NP_001073315.1:p.Arg1813Pro
NM_004380.2:c.5552G>C	NP_004371.2:p.Arg1851Pro
XM_005255124.3:c.5507G>C	XP_005255181.1:p.Arg1836Pro
XM_005255125.3:c.5135G>C	XP_005255182.1:p.Arg1712Pro
XM_006720848.2:c.5291G>C	XP_006720911.1:p.Arg1764Pro
XM_011522380.1:c.5498G>C	XP_011520682.1:p.Arg1833Pro
XM_011522381.1:c.4799G>C	XP_011520683.1:p.Arg1600Pro
XM_005255124.4:c.5507G>C	XP_005255181.1:p.Arg1836Pro
XM_005255125.4:c.5135G>C	XP_005255182.1:p.Arg1712Pro
XM_006720848.3:c.5291G>C	XP_006720911.1:p.Arg1764Pro
XM_011522381.2:c.4799G>C	XP_011520683.1:p.Arg1600Pro
XM_017022944.1:c.5546G>C	XP_016878433.1:p.Arg1849Pro
NM_004380.3:c.5552G>C MANE Select	NP_004371.2:p.Arg1851Pro