Canonical Allele Identifier: CA394554588
Gene: CREBBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3778098G>T , CM000678.2:g.3778098G>T GRCh38
NC_000016.9:g.3828099G>T , CM000678.1:g.3828099G>T GRCh37
NC_000016.8:g.3768100G>T NCBI36
NG_009873.1:g.107023C>A
NG_009873.2:g.107616C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.2026C>A MANE Select ENSP00000262367.5:p.Gln676Lys
ENST00000262367.9:c.2026C>A ENSP00000262367.5:p.Gln676Lys
ENST00000382070.7:c.1912C>A ENSP00000371502.3:p.Gln638Lys
ENST00000570939.2:c.631C>A ENSP00000461002.2:p.Gln211Lys
ENST00000571826.5:c.75C>A
ENST00000572134.1:c.339C>A
ENST00000634839.1:n.188C>A
NM_001079846.1:c.1912C>A NP_001073315.1:p.Gln638Lys
NM_004380.2:c.2026C>A NP_004371.2:p.Gln676Lys
XM_005255124.3:c.2026C>A XP_005255181.1:p.Gln676Lys
XM_005255125.3:c.2026C>A XP_005255182.1:p.Gln676Lys
XM_006720848.2:c.2026C>A XP_006720911.1:p.Gln676Lys
XM_011522380.1:c.1972C>A XP_011520682.1:p.Gln658Lys
XM_011522381.1:c.1273C>A XP_011520683.1:p.Gln425Lys
XM_011522382.1:c.2026C>A XP_011520684.1:p.Gln676Lys
XM_005255124.4:c.2026C>A XP_005255181.1:p.Gln676Lys
XM_005255125.4:c.2026C>A XP_005255182.1:p.Gln676Lys
XM_006720848.3:c.2026C>A XP_006720911.1:p.Gln676Lys
XM_011522381.2:c.1273C>A XP_011520683.1:p.Gln425Lys
XM_011522382.3:c.2026C>A XP_011520684.1:p.Gln676Lys
XM_017022944.1:c.2026C>A XP_016878433.1:p.Gln676Lys
NM_004380.3:c.2026C>A MANE Select NP_004371.2:p.Gln676Lys