Canonical Allele Identifier: CA2202936122

Gene: CREBBP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3736326_3736364delinsCCCCCCCACCACAGTGCAGCAGACCCCCACACATGTGCA , CM000678.2:g.3736326_3736364delinsCCCCCCCACCACAGTGCAGCAGACCCCCACACATGTGCA	GRCh38
NC_000016.9:g.3786327_3786365delinsCCCCCCCACCACAGTGCAGCAGACCCCCACACATGTGCA , CM000678.1:g.3786327_3786365delinsCCCCCCCACCACAGTGCAGCAGACCCCCACACATGTGCA	GRCh37
NC_000016.8:g.3726328_3726366delinsCCCCCCCACCACAGTGCAGCAGACCCCCACACATGTGCA	NCBI36
NG_009873.1:g.148757_148795delinsTGCACATGTGTGGGGGTCTGCTGCACTGTGGTGGGGGGG
NG_009873.2:g.149350_149388delinsTGCACATGTGTGGGGGTCTGCTGCACTGTGGTGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.4561-161_4561-123delinsTGCACATGTGTGGGGGTCTGCTGCACTGTGGTGGGGGGG MANE Select	ENSP00000262367.5:n.4561-161_4561-123delinsTGCACATGTGTGGGGGTC...
ENST00000262367.9:c.4561-161_4561-123delinsTGCACATGTGTGGGGGTCTGCTGCACTGTGGTGGGGGGG	ENSP00000262367.5:n.4561-161_4561-123delinsTGCACATGTGTGGGGGTC...
ENST00000382070.7:c.4447-161_4447-123delinsTGCACATGTGTGGGGGTCTGCTGCACTGTGGTGGGGGGG	ENSP00000371502.3:n.4447-161_4447-123delinsTGCACATGTGTGGGGGTC...
ENST00000570939.2:c.3196-161_3196-123delinsTGCACATGTGTGGGGGTCTGCTGCACTGTGGTGGGGGGG	ENSP00000461002.2:n.3196-161_3196-123delinsTGCACATGTGTGGGGGTC...
ENST00000571763.5:n.351-161_351-123delinsTGCACATGTGTGGGGGTCTGCTGCACTGTGGTGGGGGGG
ENST00000576720.1:n.3384-161_3384-123delinsTGCACATGTGTGGGGGTCTGCTGCACTGTGGTGGGGGGG
NM_001079846.1:c.4447-161_4447-123delinsTGCACATGTGTGGGGGTCTGCTGCACTGTGGTGGGGGGG	NP_001073315.1:n.4447-161_4447-123delinsTGCACATGTGTGGGGGTCTGC...
NM_004380.2:c.4561-161_4561-123delinsTGCACATGTGTGGGGGTCTGCTGCACTGTGGTGGGGGGG	NP_004371.2:n.4561-161_4561-123delinsTGCACATGTGTGGGGGTCTGCTGC...
XM_005255124.3:c.4516-161_4516-123delinsTGCACATGTGTGGGGGTCTGCTGCACTGTGGTGGGGGGG	XP_005255181.1:n.4516-161_4516-123delinsTGCACATGTGTGGGGGTCTGC...
XM_005255125.3:c.4144-161_4144-123delinsTGCACATGTGTGGGGGTCTGCTGCACTGTGGTGGGGGGG	XP_005255182.1:n.4144-161_4144-123delinsTGCACATGTGTGGGGGTCTGC...
XM_006720848.2:c.4300-161_4300-123delinsTGCACATGTGTGGGGGTCTGCTGCACTGTGGTGGGGGGG	XP_006720911.1:n.4300-161_4300-123delinsTGCACATGTGTGGGGGTCTGC...
XM_011522380.1:c.4507-161_4507-123delinsTGCACATGTGTGGGGGTCTGCTGCACTGTGGTGGGGGGG	XP_011520682.1:n.4507-161_4507-123delinsTGCACATGTGTGGGGGTCTGC...
XM_011522381.1:c.3808-161_3808-123delinsTGCACATGTGTGGGGGTCTGCTGCACTGTGGTGGGGGGG	XP_011520683.1:n.3808-161_3808-123delinsTGCACATGTGTGGGGGTCTGC...
XM_005255124.4:c.4516-161_4516-123delinsTGCACATGTGTGGGGGTCTGCTGCACTGTGGTGGGGGGG	XP_005255181.1:n.4516-161_4516-123delinsTGCACATGTGTGGGGGTCTGC...
XM_005255125.4:c.4144-161_4144-123delinsTGCACATGTGTGGGGGTCTGCTGCACTGTGGTGGGGGGG	XP_005255182.1:n.4144-161_4144-123delinsTGCACATGTGTGGGGGTCTGC...
XM_006720848.3:c.4300-161_4300-123delinsTGCACATGTGTGGGGGTCTGCTGCACTGTGGTGGGGGGG	XP_006720911.1:n.4300-161_4300-123delinsTGCACATGTGTGGGGGTCTGC...
XM_011522381.2:c.3808-161_3808-123delinsTGCACATGTGTGGGGGTCTGCTGCACTGTGGTGGGGGGG	XP_011520683.1:n.3808-161_3808-123delinsTGCACATGTGTGGGGGTCTGC...
XM_017022944.1:c.4555-161_4555-123delinsTGCACATGTGTGGGGGTCTGCTGCACTGTGGTGGGGGGG	XP_016878433.1:n.4555-161_4555-123delinsTGCACATGTGTGGGGGTCTGC...
NM_004380.3:c.4561-161_4561-123delinsTGCACATGTGTGGGGGTCTGCTGCACTGTGGTGGGGGGG MANE Select	NP_004371.2:n.4561-161_4561-123delinsTGCACATGTGTGGGGGTCTGCTGC...