Canonical Allele Identifier: CA2202916423

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729483A= , CM000678.2:g.3729483A=	GRCh38
NC_000016.9:g.3779484A= , CM000678.1:g.3779484A=	GRCh37
NC_000016.8:g.3719485A=	NCBI36
NG_009873.1:g.155638T=
NG_009873.2:g.156231T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5564T= MANE Select	ENSP00000262367.5:p.Ile1855=
ENST00000262367.9:c.5564T=	ENSP00000262367.5:p.Ile1855=
ENST00000382070.7:c.5450T=	ENSP00000371502.3:p.Ile1817=
NM_001079846.1:c.5450T=	NP_001073315.1:p.Ile1817=
NM_004380.2:c.5564T=	NP_004371.2:p.Ile1855=
XM_005255124.3:c.5519T=	XP_005255181.1:p.Ile1840=
XM_005255125.3:c.5147T=	XP_005255182.1:p.Ile1716=
XM_006720848.2:c.5303T=	XP_006720911.1:p.Ile1768=
XM_011522380.1:c.5510T=	XP_011520682.1:p.Ile1837=
XM_011522381.1:c.4811T=	XP_011520683.1:p.Ile1604=
XM_005255124.4:c.5519T=	XP_005255181.1:p.Ile1840=
XM_005255125.4:c.5147T=	XP_005255182.1:p.Ile1716=
XM_006720848.3:c.5303T=	XP_006720911.1:p.Ile1768=
XM_011522381.2:c.4811T=	XP_011520683.1:p.Ile1604=
XM_017022944.1:c.5558T=	XP_016878433.1:p.Ile1853=
NM_004380.3:c.5564T= MANE Select	NP_004371.2:p.Ile1855=