Canonical Allele Identifier: CA394557172

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729723C>G , CM000678.2:g.3729723C>G	GRCh38
NC_000016.9:g.3779724C>G , CM000678.1:g.3779724C>G	GRCh37
NC_000016.8:g.3719725C>G	NCBI36
NG_009873.1:g.155398G>C
NG_009873.2:g.155991G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004380.3:c.5324G>C MANE Select	NP_004371.2:p.Cys1775Ser
ENST00000262367.10:c.5324G>C MANE Select	ENSP00000262367.5:p.Cys1775Ser
NM_001079846.1:c.5210G>C	NP_001073315.1:p.Cys1737Ser
NM_004380.2:c.5324G>C	NP_004371.2:p.Cys1775Ser
ENST00000262367.9:c.5324G>C	ENSP00000262367.5:p.Cys1775Ser
ENST00000382070.7:c.5210G>C	ENSP00000371502.3:p.Cys1737Ser
XM_005255124.3:c.5279G>C	XP_005255181.1:p.Cys1760Ser
XM_005255124.4:c.5279G>C	XP_005255181.1:p.Cys1760Ser
XM_005255125.3:c.4907G>C	XP_005255182.1:p.Cys1636Ser
XM_005255125.4:c.4907G>C	XP_005255182.1:p.Cys1636Ser
XM_006720848.2:c.5063G>C	XP_006720911.1:p.Cys1688Ser
XM_006720848.3:c.5063G>C	XP_006720911.1:p.Cys1688Ser
XM_011522380.1:c.5270G>C	XP_011520682.1:p.Cys1757Ser
XM_011522381.1:c.4571G>C	XP_011520683.1:p.Cys1524Ser
XM_011522381.2:c.4571G>C	XP_011520683.1:p.Cys1524Ser
XM_017022944.1:c.5318G>C	XP_016878433.1:p.Cys1773Ser