Canonical Allele Identifier: CA394556147
Gene: CREBBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3729535A>G , CM000678.2:g.3729535A>G GRCh38
NC_000016.9:g.3779536A>G , CM000678.1:g.3779536A>G GRCh37
NC_000016.8:g.3719537A>G NCBI36
NG_009873.1:g.155586T>C
NG_009873.2:g.156179T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.5512T>C MANE Select ENSP00000262367.5:p.Cys1838Arg
ENST00000262367.9:c.5512T>C ENSP00000262367.5:p.Cys1838Arg
ENST00000382070.7:c.5398T>C ENSP00000371502.3:p.Cys1800Arg
NM_001079846.1:c.5398T>C NP_001073315.1:p.Cys1800Arg
NM_004380.2:c.5512T>C NP_004371.2:p.Cys1838Arg
XM_005255124.3:c.5467T>C XP_005255181.1:p.Cys1823Arg
XM_005255125.3:c.5095T>C XP_005255182.1:p.Cys1699Arg
XM_006720848.2:c.5251T>C XP_006720911.1:p.Cys1751Arg
XM_011522380.1:c.5458T>C XP_011520682.1:p.Cys1820Arg
XM_011522381.1:c.4759T>C XP_011520683.1:p.Cys1587Arg
XM_005255124.4:c.5467T>C XP_005255181.1:p.Cys1823Arg
XM_005255125.4:c.5095T>C XP_005255182.1:p.Cys1699Arg
XM_006720848.3:c.5251T>C XP_006720911.1:p.Cys1751Arg
XM_011522381.2:c.4759T>C XP_011520683.1:p.Cys1587Arg
XM_017022944.1:c.5506T>C XP_016878433.1:p.Cys1836Arg
NM_004380.3:c.5512T>C MANE Select NP_004371.2:p.Cys1838Arg