Canonical Allele Identifier: CA394557205
Gene: CREBBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3729730G>T , CM000678.2:g.3729730G>T GRCh38
NC_000016.9:g.3779731G>T , CM000678.1:g.3779731G>T GRCh37
NC_000016.8:g.3719732G>T NCBI36
NG_009873.1:g.155391C>A
NG_009873.2:g.155984C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.5317C>A MANE Select ENSP00000262367.5:p.Gln1773Lys
ENST00000262367.9:c.5317C>A ENSP00000262367.5:p.Gln1773Lys
ENST00000382070.7:c.5203C>A ENSP00000371502.3:p.Gln1735Lys
NM_001079846.1:c.5203C>A NP_001073315.1:p.Gln1735Lys
NM_004380.2:c.5317C>A NP_004371.2:p.Gln1773Lys
XM_005255124.3:c.5272C>A XP_005255181.1:p.Gln1758Lys
XM_005255125.3:c.4900C>A XP_005255182.1:p.Gln1634Lys
XM_006720848.2:c.5056C>A XP_006720911.1:p.Gln1686Lys
XM_011522380.1:c.5263C>A XP_011520682.1:p.Gln1755Lys
XM_011522381.1:c.4564C>A XP_011520683.1:p.Gln1522Lys
XM_005255124.4:c.5272C>A XP_005255181.1:p.Gln1758Lys
XM_005255125.4:c.4900C>A XP_005255182.1:p.Gln1634Lys
XM_006720848.3:c.5056C>A XP_006720911.1:p.Gln1686Lys
XM_011522381.2:c.4564C>A XP_011520683.1:p.Gln1522Lys
XM_017022944.1:c.5311C>A XP_016878433.1:p.Gln1771Lys
NM_004380.3:c.5317C>A MANE Select NP_004371.2:p.Gln1773Lys