Canonical Allele Identifier: CA394557177

Gene: CREBBP

Linked Data

• dbSNP Id: rs1057524802
• MyVariant Identifiers: chr16:g.3779725A>T (hg19) ; chr16:g.3729724A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729724A>T , CM000678.2:g.3729724A>T	GRCh38
NC_000016.9:g.3779725A>T , CM000678.1:g.3779725A>T	GRCh37
NC_000016.8:g.3719726A>T	NCBI36
NG_009873.1:g.155397T>A
NG_009873.2:g.155990T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000262367.10:c.5323T>A MANE Select	ENSP00000262367.5:p.Cys1775Ser
ENST00000262367.9:c.5323T>A	ENSP00000262367.5:p.Cys1775Ser
ENST00000382070.7:c.5209T>A	ENSP00000371502.3:p.Cys1737Ser
NM_001079846.1:c.5209T>A	NP_001073315.1:p.Cys1737Ser
NM_004380.2:c.5323T>A	NP_004371.2:p.Cys1775Ser
XM_005255124.3:c.5278T>A	XP_005255181.1:p.Cys1760Ser
XM_005255125.3:c.4906T>A	XP_005255182.1:p.Cys1636Ser
XM_006720848.2:c.5062T>A	XP_006720911.1:p.Cys1688Ser
XM_011522380.1:c.5269T>A	XP_011520682.1:p.Cys1757Ser
XM_011522381.1:c.4570T>A	XP_011520683.1:p.Cys1524Ser
XM_005255124.4:c.5278T>A	XP_005255181.1:p.Cys1760Ser
XM_005255125.4:c.4906T>A	XP_005255182.1:p.Cys1636Ser
XM_006720848.3:c.5062T>A	XP_006720911.1:p.Cys1688Ser
XM_011522381.2:c.4570T>A	XP_011520683.1:p.Cys1524Ser
XM_017022944.1:c.5317T>A	XP_016878433.1:p.Cys1773Ser
NM_004380.3:c.5323T>A MANE Select	NP_004371.2:p.Cys1775Ser