Canonical Allele Identifier: CA2202928430

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727973A= , CM000678.2:g.3727973A=	GRCh38
NC_000016.9:g.3777974A= , CM000678.1:g.3777974A=	GRCh37
NC_000016.8:g.3717975A=	NCBI36
NG_009873.1:g.157148T=
NG_009873.2:g.157741T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7074T= MANE Select	ENSP00000262367.5:p.Pro2358=
ENST00000262367.9:c.7074T=	ENSP00000262367.5:p.Pro2358=
ENST00000382070.7:c.6960T=	ENSP00000371502.3:p.Pro2320=
NM_001079846.1:c.6960T=	NP_001073315.1:p.Pro2320=
NM_004380.2:c.7074T=	NP_004371.2:p.Pro2358=
XM_005255124.3:c.7029T=	XP_005255181.1:p.Pro2343=
XM_005255125.3:c.6657T=	XP_005255182.1:p.Pro2219=
XM_006720848.2:c.6813T=	XP_006720911.1:p.Pro2271=
XM_011522380.1:c.7020T=	XP_011520682.1:p.Pro2340=
XM_011522381.1:c.6321T=	XP_011520683.1:p.Pro2107=
XM_005255124.4:c.7029T=	XP_005255181.1:p.Pro2343=
XM_005255125.4:c.6657T=	XP_005255182.1:p.Pro2219=
XM_006720848.3:c.6813T=	XP_006720911.1:p.Pro2271=
XM_011522381.2:c.6321T=	XP_011520683.1:p.Pro2107=
XM_017022944.1:c.7068T=	XP_016878433.1:p.Pro2356=
NM_004380.3:c.7074T= MANE Select	NP_004371.2:p.Pro2358=