Canonical Allele Identifier: CA394556146
Gene: CREBBP HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.5512T>G MANE Select ENSP00000262367.5:p.Cys1838Gly
ENST00000262367.9:c.5512T>G ENSP00000262367.5:p.Cys1838Gly
ENST00000382070.7:c.5398T>G ENSP00000371502.3:p.Cys1800Gly
NM_001079846.1:c.5398T>G NP_001073315.1:p.Cys1800Gly
NM_004380.2:c.5512T>G NP_004371.2:p.Cys1838Gly
XM_005255124.3:c.5467T>G XP_005255181.1:p.Cys1823Gly
XM_005255125.3:c.5095T>G XP_005255182.1:p.Cys1699Gly
XM_006720848.2:c.5251T>G XP_006720911.1:p.Cys1751Gly
XM_011522380.1:c.5458T>G XP_011520682.1:p.Cys1820Gly
XM_011522381.1:c.4759T>G XP_011520683.1:p.Cys1587Gly
XM_005255124.4:c.5467T>G XP_005255181.1:p.Cys1823Gly
XM_005255125.4:c.5095T>G XP_005255182.1:p.Cys1699Gly
XM_006720848.3:c.5251T>G XP_006720911.1:p.Cys1751Gly
XM_011522381.2:c.4759T>G XP_011520683.1:p.Cys1587Gly
XM_017022944.1:c.5506T>G XP_016878433.1:p.Cys1836Gly
NM_004380.3:c.5512T>G MANE Select NP_004371.2:p.Cys1838Gly