Canonical Allele Identifier: CA2202936101
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3736317_3736356delinsGCATGTGTGCCCCCCCACCACAGTGCAGCAGACCCCCACA , CM000678.2:g.3736317_3736356delinsGCATGTGTGCCCCCCCACCACAGTGCAGCAGACCCCCACA GRCh38
NC_000016.9:g.3786318_3786357delinsGCATGTGTGCCCCCCCACCACAGTGCAGCAGACCCCCACA , CM000678.1:g.3786318_3786357delinsGCATGTGTGCCCCCCCACCACAGTGCAGCAGACCCCCACA GRCh37
NC_000016.8:g.3726319_3726358delinsGCATGTGTGCCCCCCCACCACAGTGCAGCAGACCCCCACA NCBI36
NG_009873.1:g.148765_148804delinsTGTGGGGGTCTGCTGCACTGTGGTGGGGGGGCACACATGC
NG_009873.2:g.149358_149397delinsTGTGGGGGTCTGCTGCACTGTGGTGGGGGGGCACACATGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.4561-153_4561-114delinsTGTGGGGGTCTGCTGCACTGTGGTGGGGGGGCACACATGC MANE Select ENSP00000262367.5:n.4561-153_4561-114delinsTGTGGGGGTCTGCTGCAC...
ENST00000262367.9:c.4561-153_4561-114delinsTGTGGGGGTCTGCTGCACTGTGGTGGGGGGGCACACATGC ENSP00000262367.5:n.4561-153_4561-114delinsTGTGGGGGTCTGCTGCAC...
ENST00000382070.7:c.4447-153_4447-114delinsTGTGGGGGTCTGCTGCACTGTGGTGGGGGGGCACACATGC ENSP00000371502.3:n.4447-153_4447-114delinsTGTGGGGGTCTGCTGCAC...
ENST00000570939.2:c.3196-153_3196-114delinsTGTGGGGGTCTGCTGCACTGTGGTGGGGGGGCACACATGC ENSP00000461002.2:n.3196-153_3196-114delinsTGTGGGGGTCTGCTGCAC...
ENST00000571763.5:n.351-153_351-114delinsTGTGGGGGTCTGCTGCACTGTGGTGGGGGGGCACACATGC
ENST00000576720.1:n.3384-153_3384-114delinsTGTGGGGGTCTGCTGCACTGTGGTGGGGGGGCACACATGC
NM_001079846.1:c.4447-153_4447-114delinsTGTGGGGGTCTGCTGCACTGTGGTGGGGGGGCACACATGC NP_001073315.1:n.4447-153_4447-114delinsTGTGGGGGTCTGCTGCACTGT...
NM_004380.2:c.4561-153_4561-114delinsTGTGGGGGTCTGCTGCACTGTGGTGGGGGGGCACACATGC NP_004371.2:n.4561-153_4561-114delinsTGTGGGGGTCTGCTGCACTGTGGT...
XM_005255124.3:c.4516-153_4516-114delinsTGTGGGGGTCTGCTGCACTGTGGTGGGGGGGCACACATGC XP_005255181.1:n.4516-153_4516-114delinsTGTGGGGGTCTGCTGCACTGT...
XM_005255125.3:c.4144-153_4144-114delinsTGTGGGGGTCTGCTGCACTGTGGTGGGGGGGCACACATGC XP_005255182.1:n.4144-153_4144-114delinsTGTGGGGGTCTGCTGCACTGT...
XM_006720848.2:c.4300-153_4300-114delinsTGTGGGGGTCTGCTGCACTGTGGTGGGGGGGCACACATGC XP_006720911.1:n.4300-153_4300-114delinsTGTGGGGGTCTGCTGCACTGT...
XM_011522380.1:c.4507-153_4507-114delinsTGTGGGGGTCTGCTGCACTGTGGTGGGGGGGCACACATGC XP_011520682.1:n.4507-153_4507-114delinsTGTGGGGGTCTGCTGCACTGT...
XM_011522381.1:c.3808-153_3808-114delinsTGTGGGGGTCTGCTGCACTGTGGTGGGGGGGCACACATGC XP_011520683.1:n.3808-153_3808-114delinsTGTGGGGGTCTGCTGCACTGT...
XM_005255124.4:c.4516-153_4516-114delinsTGTGGGGGTCTGCTGCACTGTGGTGGGGGGGCACACATGC XP_005255181.1:n.4516-153_4516-114delinsTGTGGGGGTCTGCTGCACTGT...
XM_005255125.4:c.4144-153_4144-114delinsTGTGGGGGTCTGCTGCACTGTGGTGGGGGGGCACACATGC XP_005255182.1:n.4144-153_4144-114delinsTGTGGGGGTCTGCTGCACTGT...
XM_006720848.3:c.4300-153_4300-114delinsTGTGGGGGTCTGCTGCACTGTGGTGGGGGGGCACACATGC XP_006720911.1:n.4300-153_4300-114delinsTGTGGGGGTCTGCTGCACTGT...
XM_011522381.2:c.3808-153_3808-114delinsTGTGGGGGTCTGCTGCACTGTGGTGGGGGGGCACACATGC XP_011520683.1:n.3808-153_3808-114delinsTGTGGGGGTCTGCTGCACTGT...
XM_017022944.1:c.4555-153_4555-114delinsTGTGGGGGTCTGCTGCACTGTGGTGGGGGGGCACACATGC XP_016878433.1:n.4555-153_4555-114delinsTGTGGGGGTCTGCTGCACTGT...
NM_004380.3:c.4561-153_4561-114delinsTGTGGGGGTCTGCTGCACTGTGGTGGGGGGGCACACATGC MANE Select NP_004371.2:n.4561-153_4561-114delinsTGTGGGGGTCTGCTGCACTGTGGT...