Canonical Allele Identifier: CA394563559
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs2151329435

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3736703A>T , CM000678.2:g.3736703A>T GRCh38
NC_000016.9:g.3786704A>T , CM000678.1:g.3786704A>T GRCh37
NC_000016.8:g.3726705A>T NCBI36
NG_009873.1:g.148418T>A
NG_009873.2:g.149011T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.4507T>A MANE Select ENSP00000262367.5:p.Tyr1503Asn
ENST00000262367.9:c.4507T>A ENSP00000262367.5:p.Tyr1503Asn
ENST00000382070.7:c.4393T>A ENSP00000371502.3:p.Tyr1465Asn
ENST00000570939.2:c.3142T>A ENSP00000461002.2:p.Tyr1048Asn
ENST00000571763.5:n.297T>A
ENST00000574740.1:n.328T>A
ENST00000576720.1:n.3330T>A
NM_001079846.1:c.4393T>A NP_001073315.1:p.Tyr1465Asn
NM_004380.2:c.4507T>A NP_004371.2:p.Tyr1503Asn
XM_005255124.3:c.4462T>A XP_005255181.1:p.Tyr1488Asn
XM_005255125.3:c.4090T>A XP_005255182.1:p.Tyr1364Asn
XM_006720848.2:c.4246T>A XP_006720911.1:p.Tyr1416Asn
XM_011522380.1:c.4453T>A XP_011520682.1:p.Tyr1485Asn
XM_011522381.1:c.3754T>A XP_011520683.1:p.Tyr1252Asn
XM_005255124.4:c.4462T>A XP_005255181.1:p.Tyr1488Asn
XM_005255125.4:c.4090T>A XP_005255182.1:p.Tyr1364Asn
XM_006720848.3:c.4246T>A XP_006720911.1:p.Tyr1416Asn
XM_011522381.2:c.3754T>A XP_011520683.1:p.Tyr1252Asn
XM_017022944.1:c.4501T>A XP_016878433.1:p.Tyr1501Asn
NM_004380.3:c.4507T>A MANE Select NP_004371.2:p.Tyr1503Asn