Canonical Allele Identifier: CA2202936695

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3736766A= , CM000678.2:g.3736766A=	GRCh38
NC_000016.9:g.3786767A= , CM000678.1:g.3786767A=	GRCh37
NC_000016.8:g.3726768A=	NCBI36
NG_009873.1:g.148355T=
NG_009873.2:g.148948T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.4444T= MANE Select	ENSP00000262367.5:p.Tyr1482=
ENST00000262367.9:c.4444T=	ENSP00000262367.5:p.Tyr1482=
ENST00000382070.7:c.4330T=	ENSP00000371502.3:p.Tyr1444=
ENST00000570939.2:c.3079T=	ENSP00000461002.2:p.Tyr1027=
ENST00000571763.5:n.234T=
ENST00000574740.1:n.265T=
ENST00000576720.1:n.3267T=
NM_001079846.1:c.4330T=	NP_001073315.1:p.Tyr1444=
NM_004380.2:c.4444T=	NP_004371.2:p.Tyr1482=
XM_005255124.3:c.4399T=	XP_005255181.1:p.Tyr1467=
XM_005255125.3:c.4027T=	XP_005255182.1:p.Tyr1343=
XM_006720848.2:c.4183T=	XP_006720911.1:p.Tyr1395=
XM_011522380.1:c.4390T=	XP_011520682.1:p.Tyr1464=
XM_011522381.1:c.3691T=	XP_011520683.1:p.Tyr1231=
XM_005255124.4:c.4399T=	XP_005255181.1:p.Tyr1467=
XM_005255125.4:c.4027T=	XP_005255182.1:p.Tyr1343=
XM_006720848.3:c.4183T=	XP_006720911.1:p.Tyr1395=
XM_011522381.2:c.3691T=	XP_011520683.1:p.Tyr1231=
XM_017022944.1:c.4438T=	XP_016878433.1:p.Tyr1480=
NM_004380.3:c.4444T= MANE Select	NP_004371.2:p.Tyr1482=