Canonical Allele Identifier: CA394556533

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3779641G>T (hg19) ; chr16:g.3729640G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729640G>T , CM000678.2:g.3729640G>T	GRCh38
NC_000016.9:g.3779641G>T , CM000678.1:g.3779641G>T	GRCh37
NC_000016.8:g.3719642G>T	NCBI36
NG_009873.1:g.155481C>A
NG_009873.2:g.156074C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5407C>A MANE Select	ENSP00000262367.5:p.Gln1803Lys
ENST00000262367.9:c.5407C>A	ENSP00000262367.5:p.Gln1803Lys
ENST00000382070.7:c.5293C>A	ENSP00000371502.3:p.Gln1765Lys
NM_001079846.1:c.5293C>A	NP_001073315.1:p.Gln1765Lys
NM_004380.2:c.5407C>A	NP_004371.2:p.Gln1803Lys
XM_005255124.3:c.5362C>A	XP_005255181.1:p.Gln1788Lys
XM_005255125.3:c.4990C>A	XP_005255182.1:p.Gln1664Lys
XM_006720848.2:c.5146C>A	XP_006720911.1:p.Gln1716Lys
XM_011522380.1:c.5353C>A	XP_011520682.1:p.Gln1785Lys
XM_011522381.1:c.4654C>A	XP_011520683.1:p.Gln1552Lys
XM_005255124.4:c.5362C>A	XP_005255181.1:p.Gln1788Lys
XM_005255125.4:c.4990C>A	XP_005255182.1:p.Gln1664Lys
XM_006720848.3:c.5146C>A	XP_006720911.1:p.Gln1716Lys
XM_011522381.2:c.4654C>A	XP_011520683.1:p.Gln1552Lys
XM_017022944.1:c.5401C>A	XP_016878433.1:p.Gln1801Lys
NM_004380.3:c.5407C>A MANE Select	NP_004371.2:p.Gln1803Lys