Canonical Allele Identifier: CA2202916154

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729001T= , CM000678.2:g.3729001T=	GRCh38
NC_000016.9:g.3779002T= , CM000678.1:g.3779002T=	GRCh37
NC_000016.8:g.3719003T=	NCBI36
NG_009873.1:g.156120A=
NG_009873.2:g.156713A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6046A= MANE Select	ENSP00000262367.5:p.Met2016=
ENST00000262367.9:c.6046A=	ENSP00000262367.5:p.Met2016=
ENST00000382070.7:c.5932A=	ENSP00000371502.3:p.Met1978=
NM_001079846.1:c.5932A=	NP_001073315.1:p.Met1978=
NM_004380.2:c.6046A=	NP_004371.2:p.Met2016=
XM_005255124.3:c.6001A=	XP_005255181.1:p.Met2001=
XM_005255125.3:c.5629A=	XP_005255182.1:p.Met1877=
XM_006720848.2:c.5785A=	XP_006720911.1:p.Met1929=
XM_011522380.1:c.5992A=	XP_011520682.1:p.Met1998=
XM_011522381.1:c.5293A=	XP_011520683.1:p.Met1765=
XM_005255124.4:c.6001A=	XP_005255181.1:p.Met2001=
XM_005255125.4:c.5629A=	XP_005255182.1:p.Met1877=
XM_006720848.3:c.5785A=	XP_006720911.1:p.Met1929=
XM_011522381.2:c.5293A=	XP_011520683.1:p.Met1765=
XM_017022944.1:c.6040A=	XP_016878433.1:p.Met2014=
NM_004380.3:c.6046A= MANE Select	NP_004371.2:p.Met2016=