Canonical Allele Identifier: CA2202928480

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728106A= , CM000678.2:g.3728106A=	GRCh38
NC_000016.9:g.3778107A= , CM000678.1:g.3778107A=	GRCh37
NC_000016.8:g.3718108A=	NCBI36
NG_009873.1:g.157015T=
NG_009873.2:g.157608T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6941T= MANE Select	ENSP00000262367.5:p.Met2314=
ENST00000262367.9:c.6941T=	ENSP00000262367.5:p.Met2314=
ENST00000382070.7:c.6827T=	ENSP00000371502.3:p.Met2276=
NM_001079846.1:c.6827T=	NP_001073315.1:p.Met2276=
NM_004380.2:c.6941T=	NP_004371.2:p.Met2314=
XM_005255124.3:c.6896T=	XP_005255181.1:p.Met2299=
XM_005255125.3:c.6524T=	XP_005255182.1:p.Met2175=
XM_006720848.2:c.6680T=	XP_006720911.1:p.Met2227=
XM_011522380.1:c.6887T=	XP_011520682.1:p.Met2296=
XM_011522381.1:c.6188T=	XP_011520683.1:p.Met2063=
XM_005255124.4:c.6896T=	XP_005255181.1:p.Met2299=
XM_005255125.4:c.6524T=	XP_005255182.1:p.Met2175=
XM_006720848.3:c.6680T=	XP_006720911.1:p.Met2227=
XM_011522381.2:c.6188T=	XP_011520683.1:p.Met2063=
XM_017022944.1:c.6935T=	XP_016878433.1:p.Met2312=
NM_004380.3:c.6941T= MANE Select	NP_004371.2:p.Met2314=