Canonical Allele Identifier: CA394554529
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs1388175135

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3778086C>G , CM000678.2:g.3778086C>G GRCh38
NC_000016.9:g.3828087C>G , CM000678.1:g.3828087C>G GRCh37
NC_000016.8:g.3768088C>G NCBI36
NG_009873.1:g.107035G>C
NG_009873.2:g.107628G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.2038G>C MANE Select ENSP00000262367.5:p.Gly680Arg
ENST00000262367.9:c.2038G>C ENSP00000262367.5:p.Gly680Arg
ENST00000382070.7:c.1924G>C ENSP00000371502.3:p.Gly642Arg
ENST00000570939.2:c.643G>C ENSP00000461002.2:p.Gly215Arg
ENST00000571826.5:c.87G>C
ENST00000572134.1:c.351G>C
ENST00000634839.1:n.200G>C
NM_001079846.1:c.1924G>C NP_001073315.1:p.Gly642Arg
NM_004380.2:c.2038G>C NP_004371.2:p.Gly680Arg
XM_005255124.3:c.2038G>C XP_005255181.1:p.Gly680Arg
XM_005255125.3:c.2038G>C XP_005255182.1:p.Gly680Arg
XM_006720848.2:c.2038G>C XP_006720911.1:p.Gly680Arg
XM_011522380.1:c.1984G>C XP_011520682.1:p.Gly662Arg
XM_011522381.1:c.1285G>C XP_011520683.1:p.Gly429Arg
XM_011522382.1:c.2038G>C XP_011520684.1:p.Gly680Arg
XM_005255124.4:c.2038G>C XP_005255181.1:p.Gly680Arg
XM_005255125.4:c.2038G>C XP_005255182.1:p.Gly680Arg
XM_006720848.3:c.2038G>C XP_006720911.1:p.Gly680Arg
XM_011522381.2:c.1285G>C XP_011520683.1:p.Gly429Arg
XM_011522382.3:c.2038G>C XP_011520684.1:p.Gly680Arg
XM_017022944.1:c.2038G>C XP_016878433.1:p.Gly680Arg
NM_004380.3:c.2038G>C MANE Select NP_004371.2:p.Gly680Arg