Canonical Allele Identifier: CA2202928885

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728869T= , CM000678.2:g.3728869T=	GRCh38
NC_000016.9:g.3778870T= , CM000678.1:g.3778870T=	GRCh37
NC_000016.8:g.3718871T=	NCBI36
NG_009873.1:g.156252A=
NG_009873.2:g.156845A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6178A= MANE Select	ENSP00000262367.5:p.Arg2060=
ENST00000262367.9:c.6178A=	ENSP00000262367.5:p.Arg2060=
ENST00000382070.7:c.6064A=	ENSP00000371502.3:p.Arg2022=
NM_001079846.1:c.6064A=	NP_001073315.1:p.Arg2022=
NM_004380.2:c.6178A=	NP_004371.2:p.Arg2060=
XM_005255124.3:c.6133A=	XP_005255181.1:p.Arg2045=
XM_005255125.3:c.5761A=	XP_005255182.1:p.Arg1921=
XM_006720848.2:c.5917A=	XP_006720911.1:p.Arg1973=
XM_011522380.1:c.6124A=	XP_011520682.1:p.Arg2042=
XM_011522381.1:c.5425A=	XP_011520683.1:p.Arg1809=
XM_005255124.4:c.6133A=	XP_005255181.1:p.Arg2045=
XM_005255125.4:c.5761A=	XP_005255182.1:p.Arg1921=
XM_006720848.3:c.5917A=	XP_006720911.1:p.Arg1973=
XM_011522381.2:c.5425A=	XP_011520683.1:p.Arg1809=
XM_017022944.1:c.6172A=	XP_016878433.1:p.Arg2058=
NM_004380.3:c.6178A= MANE Select	NP_004371.2:p.Arg2060=