Canonical Allele Identifier: CA394556142
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs2151310249

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3729533G>T , CM000678.2:g.3729533G>T GRCh38
NC_000016.9:g.3779534G>T , CM000678.1:g.3779534G>T GRCh37
NC_000016.8:g.3719535G>T NCBI36
NG_009873.1:g.155588C>A
NG_009873.2:g.156181C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.5514C>A MANE Select ENSP00000262367.5:p.Cys1838Ter
ENST00000262367.9:c.5514C>A ENSP00000262367.5:p.Cys1838Ter
ENST00000382070.7:c.5400C>A ENSP00000371502.3:p.Cys1800Ter
NM_001079846.1:c.5400C>A NP_001073315.1:p.Cys1800Ter
NM_004380.2:c.5514C>A NP_004371.2:p.Cys1838Ter
XM_005255124.3:c.5469C>A XP_005255181.1:p.Cys1823Ter
XM_005255125.3:c.5097C>A XP_005255182.1:p.Cys1699Ter
XM_006720848.2:c.5253C>A XP_006720911.1:p.Cys1751Ter
XM_011522380.1:c.5460C>A XP_011520682.1:p.Cys1820Ter
XM_011522381.1:c.4761C>A XP_011520683.1:p.Cys1587Ter
XM_005255124.4:c.5469C>A XP_005255181.1:p.Cys1823Ter
XM_005255125.4:c.5097C>A XP_005255182.1:p.Cys1699Ter
XM_006720848.3:c.5253C>A XP_006720911.1:p.Cys1751Ter
XM_011522381.2:c.4761C>A XP_011520683.1:p.Cys1587Ter
XM_017022944.1:c.5508C>A XP_016878433.1:p.Cys1836Ter
NM_004380.3:c.5514C>A MANE Select NP_004371.2:p.Cys1838Ter