Canonical Allele Identifier: CA2202916152

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728995G= , CM000678.2:g.3728995G=	GRCh38
NC_000016.9:g.3778996G= , CM000678.1:g.3778996G=	GRCh37
NC_000016.8:g.3718997G=	NCBI36
NG_009873.1:g.156126C=
NG_009873.2:g.156719C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6052C= MANE Select	ENSP00000262367.5:p.Pro2018=
ENST00000262367.9:c.6052C=	ENSP00000262367.5:p.Pro2018=
ENST00000382070.7:c.5938C=	ENSP00000371502.3:p.Pro1980=
NM_001079846.1:c.5938C=	NP_001073315.1:p.Pro1980=
NM_004380.2:c.6052C=	NP_004371.2:p.Pro2018=
XM_005255124.3:c.6007C=	XP_005255181.1:p.Pro2003=
XM_005255125.3:c.5635C=	XP_005255182.1:p.Pro1879=
XM_006720848.2:c.5791C=	XP_006720911.1:p.Pro1931=
XM_011522380.1:c.5998C=	XP_011520682.1:p.Pro2000=
XM_011522381.1:c.5299C=	XP_011520683.1:p.Pro1767=
XM_005255124.4:c.6007C=	XP_005255181.1:p.Pro2003=
XM_005255125.4:c.5635C=	XP_005255182.1:p.Pro1879=
XM_006720848.3:c.5791C=	XP_006720911.1:p.Pro1931=
XM_011522381.2:c.5299C=	XP_011520683.1:p.Pro1767=
XM_017022944.1:c.6046C=	XP_016878433.1:p.Pro2016=
NM_004380.3:c.6052C= MANE Select	NP_004371.2:p.Pro2018=