Canonical Allele Identifier: CA2202958681

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3778039A= , CM000678.2:g.3778039A=	GRCh38
NC_000016.9:g.3828040A= , CM000678.1:g.3828040A=	GRCh37
NC_000016.8:g.3768041A=	NCBI36
NG_009873.1:g.107082T=
NG_009873.2:g.107675T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.2085T= MANE Select	ENSP00000262367.5:p.Ile695=
ENST00000262367.9:c.2085T=	ENSP00000262367.5:p.Ile695=
ENST00000382070.7:c.1971T=	ENSP00000371502.3:p.Ile657=
ENST00000570939.2:c.690T=	ENSP00000461002.2:p.Ile230=
ENST00000571826.5:c.134T=
ENST00000572134.1:c.398T=
ENST00000634839.1:n.247T=
NM_001079846.1:c.1971T=	NP_001073315.1:p.Ile657=
NM_004380.2:c.2085T=	NP_004371.2:p.Ile695=
XM_005255124.3:c.2085T=	XP_005255181.1:p.Ile695=
XM_005255125.3:c.2085T=	XP_005255182.1:p.Ile695=
XM_006720848.2:c.2085T=	XP_006720911.1:p.Ile695=
XM_011522380.1:c.2031T=	XP_011520682.1:p.Ile677=
XM_011522381.1:c.1332T=	XP_011520683.1:p.Ile444=
XM_011522382.1:c.2085T=	XP_011520684.1:p.Ile695=
XM_005255124.4:c.2085T=	XP_005255181.1:p.Ile695=
XM_005255125.4:c.2085T=	XP_005255182.1:p.Ile695=
XM_006720848.3:c.2085T=	XP_006720911.1:p.Ile695=
XM_011522381.2:c.1332T=	XP_011520683.1:p.Ile444=
XM_011522382.3:c.2085T=	XP_011520684.1:p.Ile695=
XM_017022944.1:c.2085T=	XP_016878433.1:p.Ile695=
NM_004380.3:c.2085T= MANE Select	NP_004371.2:p.Ile695=