Canonical Allele Identifier: CA394554318
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs1435888013

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3778032C>G , CM000678.2:g.3778032C>G GRCh38
NC_000016.9:g.3828033C>G , CM000678.1:g.3828033C>G GRCh37
NC_000016.8:g.3768034C>G NCBI36
NG_009873.1:g.107089G>C
NG_009873.2:g.107682G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.2092G>C MANE Select ENSP00000262367.5:p.Ala698Pro
ENST00000262367.9:c.2092G>C ENSP00000262367.5:p.Ala698Pro
ENST00000382070.7:c.1978G>C ENSP00000371502.3:p.Ala660Pro
ENST00000570939.2:c.697G>C ENSP00000461002.2:p.Ala233Pro
ENST00000571826.5:c.141G>C
ENST00000572134.1:c.405G>C
ENST00000634839.1:n.254G>C
NM_001079846.1:c.1978G>C NP_001073315.1:p.Ala660Pro
NM_004380.2:c.2092G>C NP_004371.2:p.Ala698Pro
XM_005255124.3:c.2092G>C XP_005255181.1:p.Ala698Pro
XM_005255125.3:c.2092G>C XP_005255182.1:p.Ala698Pro
XM_006720848.2:c.2092G>C XP_006720911.1:p.Ala698Pro
XM_011522380.1:c.2038G>C XP_011520682.1:p.Ala680Pro
XM_011522381.1:c.1339G>C XP_011520683.1:p.Ala447Pro
XM_011522382.1:c.2092G>C XP_011520684.1:p.Ala698Pro
XM_005255124.4:c.2092G>C XP_005255181.1:p.Ala698Pro
XM_005255125.4:c.2092G>C XP_005255182.1:p.Ala698Pro
XM_006720848.3:c.2092G>C XP_006720911.1:p.Ala698Pro
XM_011522381.2:c.1339G>C XP_011520683.1:p.Ala447Pro
XM_011522382.3:c.2092G>C XP_011520684.1:p.Ala698Pro
XM_017022944.1:c.2092G>C XP_016878433.1:p.Ala698Pro
NM_004380.3:c.2092G>C MANE Select NP_004371.2:p.Ala698Pro