Canonical Allele Identifier: CA2202936692

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3736765T= , CM000678.2:g.3736765T=	GRCh38
NC_000016.9:g.3786766T= , CM000678.1:g.3786766T=	GRCh37
NC_000016.8:g.3726767T=	NCBI36
NG_009873.1:g.148356A=
NG_009873.2:g.148949A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.4445A= MANE Select	ENSP00000262367.5:p.Tyr1482=
ENST00000262367.9:c.4445A=	ENSP00000262367.5:p.Tyr1482=
ENST00000382070.7:c.4331A=	ENSP00000371502.3:p.Tyr1444=
ENST00000570939.2:c.3080A=	ENSP00000461002.2:p.Tyr1027=
ENST00000571763.5:n.235A=
ENST00000574740.1:n.266A=
ENST00000576720.1:n.3268A=
NM_001079846.1:c.4331A=	NP_001073315.1:p.Tyr1444=
NM_004380.2:c.4445A=	NP_004371.2:p.Tyr1482=
XM_005255124.3:c.4400A=	XP_005255181.1:p.Tyr1467=
XM_005255125.3:c.4028A=	XP_005255182.1:p.Tyr1343=
XM_006720848.2:c.4184A=	XP_006720911.1:p.Tyr1395=
XM_011522380.1:c.4391A=	XP_011520682.1:p.Tyr1464=
XM_011522381.1:c.3692A=	XP_011520683.1:p.Tyr1231=
XM_005255124.4:c.4400A=	XP_005255181.1:p.Tyr1467=
XM_005255125.4:c.4028A=	XP_005255182.1:p.Tyr1343=
XM_006720848.3:c.4184A=	XP_006720911.1:p.Tyr1395=
XM_011522381.2:c.3692A=	XP_011520683.1:p.Tyr1231=
XM_017022944.1:c.4439A=	XP_016878433.1:p.Tyr1480=
NM_004380.3:c.4445A= MANE Select	NP_004371.2:p.Tyr1482=