Canonical Allele Identifier: CA2202916934

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729997A= , CM000678.2:g.3729997A=	GRCh38
NC_000016.9:g.3779998A= , CM000678.1:g.3779998A=	GRCh37
NC_000016.8:g.3719999A=	NCBI36
NG_009873.1:g.155124T=
NG_009873.2:g.155717T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5173-123T= MANE Select	ENSP00000262367.5:n.5173-123T=
ENST00000262367.9:c.5173-123T=	ENSP00000262367.5:n.5173-123T=
ENST00000382070.7:c.5059-123T=	ENSP00000371502.3:n.5059-123T=
NM_001079846.1:c.5059-123T=	NP_001073315.1:n.5059-123T=
NM_004380.2:c.5173-123T=	NP_004371.2:n.5173-123T=
XM_005255124.3:c.5128-123T=	XP_005255181.1:n.5128-123T=
XM_005255125.3:c.4756-123T=	XP_005255182.1:n.4756-123T=
XM_006720848.2:c.4912-123T=	XP_006720911.1:n.4912-123T=
XM_011522380.1:c.5119-123T=	XP_011520682.1:n.5119-123T=
XM_011522381.1:c.4420-123T=	XP_011520683.1:n.4420-123T=
XM_005255124.4:c.5128-123T=	XP_005255181.1:n.5128-123T=
XM_005255125.4:c.4756-123T=	XP_005255182.1:n.4756-123T=
XM_006720848.3:c.4912-123T=	XP_006720911.1:n.4912-123T=
XM_011522381.2:c.4420-123T=	XP_011520683.1:n.4420-123T=
XM_017022944.1:c.5167-123T=	XP_016878433.1:n.5167-123T=
NM_004380.3:c.5173-123T= MANE Select	NP_004371.2:n.5173-123T=