Canonical Allele Identifier: CA2202953604

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3791984G= , CM000678.2:g.3791984G=	GRCh38
NC_000016.9:g.3841985G= , CM000678.1:g.3841985G=	GRCh37
NC_000016.8:g.3781986G=	NCBI36
NG_009873.1:g.93137C=
NG_009873.2:g.93730C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.1327C= MANE Select	ENSP00000262367.5:p.Gln443=
ENST00000262367.9:c.1327C=	ENSP00000262367.5:p.Gln443=
ENST00000382070.7:c.1216+1402C=	ENSP00000371502.3:n.1216+1402C=
NM_001079846.1:c.1216+1402C=	NP_001073315.1:n.1216+1402C=
NM_004380.2:c.1327C=	NP_004371.2:p.Gln443=
XM_005255124.3:c.1327C=	XP_005255181.1:p.Gln443=
XM_005255125.3:c.1327C=	XP_005255182.1:p.Gln443=
XM_006720848.2:c.1327C=	XP_006720911.1:p.Gln443=
XM_011522380.1:c.1273C=	XP_011520682.1:p.Gln425=
XM_011522381.1:c.574C=	XP_011520683.1:p.Gln192=
XM_011522382.1:c.1327C=	XP_011520684.1:p.Gln443=
XM_005255124.4:c.1327C=	XP_005255181.1:p.Gln443=
XM_005255125.4:c.1327C=	XP_005255182.1:p.Gln443=
XM_006720848.3:c.1327C=	XP_006720911.1:p.Gln443=
XM_011522381.2:c.574C=	XP_011520683.1:p.Gln192=
XM_011522382.3:c.1327C=	XP_011520684.1:p.Gln443=
XM_017022944.1:c.1327C=	XP_016878433.1:p.Gln443=
NM_004380.3:c.1327C= MANE Select	NP_004371.2:p.Gln443=