Canonical Allele Identifier: CA394556140
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs2151310236

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3729532G>T , CM000678.2:g.3729532G>T GRCh38
NC_000016.9:g.3779533G>T , CM000678.1:g.3779533G>T GRCh37
NC_000016.8:g.3719534G>T NCBI36
NG_009873.1:g.155589C>A
NG_009873.2:g.156182C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.5515C>A MANE Select ENSP00000262367.5:p.Pro1839Thr
ENST00000262367.9:c.5515C>A ENSP00000262367.5:p.Pro1839Thr
ENST00000382070.7:c.5401C>A ENSP00000371502.3:p.Pro1801Thr
NM_001079846.1:c.5401C>A NP_001073315.1:p.Pro1801Thr
NM_004380.2:c.5515C>A NP_004371.2:p.Pro1839Thr
XM_005255124.3:c.5470C>A XP_005255181.1:p.Pro1824Thr
XM_005255125.3:c.5098C>A XP_005255182.1:p.Pro1700Thr
XM_006720848.2:c.5254C>A XP_006720911.1:p.Pro1752Thr
XM_011522380.1:c.5461C>A XP_011520682.1:p.Pro1821Thr
XM_011522381.1:c.4762C>A XP_011520683.1:p.Pro1588Thr
XM_005255124.4:c.5470C>A XP_005255181.1:p.Pro1824Thr
XM_005255125.4:c.5098C>A XP_005255182.1:p.Pro1700Thr
XM_006720848.3:c.5254C>A XP_006720911.1:p.Pro1752Thr
XM_011522381.2:c.4762C>A XP_011520683.1:p.Pro1588Thr
XM_017022944.1:c.5509C>A XP_016878433.1:p.Pro1837Thr
NM_004380.3:c.5515C>A MANE Select NP_004371.2:p.Pro1839Thr