Canonical Allele Identifier: CA394554545

Gene: CREBBP

Linked Data

• gnomAD v4: 16-3729021-C-A
• MyVariant Identifiers: chr16:g.3779022C>A (hg19) ; chr16:g.3729021C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729021C>A , CM000678.2:g.3729021C>A	GRCh38
NC_000016.9:g.3779022C>A , CM000678.1:g.3779022C>A	GRCh37
NC_000016.8:g.3719023C>A	NCBI36
NG_009873.1:g.156100G>T
NG_009873.2:g.156693G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6026G>T MANE Select	ENSP00000262367.5:p.Ser2009Ile
ENST00000262367.9:c.6026G>T	ENSP00000262367.5:p.Ser2009Ile
ENST00000382070.7:c.5912G>T	ENSP00000371502.3:p.Ser1971Ile
NM_001079846.1:c.5912G>T	NP_001073315.1:p.Ser1971Ile
NM_004380.2:c.6026G>T	NP_004371.2:p.Ser2009Ile
XM_005255124.3:c.5981G>T	XP_005255181.1:p.Ser1994Ile
XM_005255125.3:c.5609G>T	XP_005255182.1:p.Ser1870Ile
XM_006720848.2:c.5765G>T	XP_006720911.1:p.Ser1922Ile
XM_011522380.1:c.5972G>T	XP_011520682.1:p.Ser1991Ile
XM_011522381.1:c.5273G>T	XP_011520683.1:p.Ser1758Ile
XM_005255124.4:c.5981G>T	XP_005255181.1:p.Ser1994Ile
XM_005255125.4:c.5609G>T	XP_005255182.1:p.Ser1870Ile
XM_006720848.3:c.5765G>T	XP_006720911.1:p.Ser1922Ile
XM_011522381.2:c.5273G>T	XP_011520683.1:p.Ser1758Ile
XM_017022944.1:c.6020G>T	XP_016878433.1:p.Ser2007Ile
NM_004380.3:c.6026G>T MANE Select	NP_004371.2:p.Ser2009Ile