Canonical Allele Identifier: CA394563296
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs2151329135

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3736659A>T , CM000678.2:g.3736659A>T GRCh38
NC_000016.9:g.3786660A>T , CM000678.1:g.3786660A>T GRCh37
NC_000016.8:g.3726661A>T NCBI36
NG_009873.1:g.148462T>A
NG_009873.2:g.149055T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.4551T>A MANE Select ENSP00000262367.5:p.His1517Gln
ENST00000262367.9:c.4551T>A ENSP00000262367.5:p.His1517Gln
ENST00000382070.7:c.4437T>A ENSP00000371502.3:p.His1479Gln
ENST00000570939.2:c.3186T>A ENSP00000461002.2:p.His1062Gln
ENST00000571763.5:n.341T>A
ENST00000574740.1:n.372T>A
ENST00000576720.1:n.3374T>A
NM_001079846.1:c.4437T>A NP_001073315.1:p.His1479Gln
NM_004380.2:c.4551T>A NP_004371.2:p.His1517Gln
XM_005255124.3:c.4506T>A XP_005255181.1:p.His1502Gln
XM_005255125.3:c.4134T>A XP_005255182.1:p.His1378Gln
XM_006720848.2:c.4290T>A XP_006720911.1:p.His1430Gln
XM_011522380.1:c.4497T>A XP_011520682.1:p.His1499Gln
XM_011522381.1:c.3798T>A XP_011520683.1:p.His1266Gln
XM_005255124.4:c.4506T>A XP_005255181.1:p.His1502Gln
XM_005255125.4:c.4134T>A XP_005255182.1:p.His1378Gln
XM_006720848.3:c.4290T>A XP_006720911.1:p.His1430Gln
XM_011522381.2:c.3798T>A XP_011520683.1:p.His1266Gln
XM_017022944.1:c.4545T>A XP_016878433.1:p.His1515Gln
NM_004380.3:c.4551T>A MANE Select NP_004371.2:p.His1517Gln