Canonical Allele Identifier: CA394553824
Gene: CREBBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3728805T>G , CM000678.2:g.3728805T>G GRCh38
NC_000016.9:g.3778806T>G , CM000678.1:g.3778806T>G GRCh37
NC_000016.8:g.3718807T>G NCBI36
NG_009873.1:g.156316A>C
NG_009873.2:g.156909A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.6242A>C MANE Select ENSP00000262367.5:p.Gln2081Pro
ENST00000262367.9:c.6242A>C ENSP00000262367.5:p.Gln2081Pro
ENST00000382070.7:c.6128A>C ENSP00000371502.3:p.Gln2043Pro
NM_001079846.1:c.6128A>C NP_001073315.1:p.Gln2043Pro
NM_004380.2:c.6242A>C NP_004371.2:p.Gln2081Pro
XM_005255124.3:c.6197A>C XP_005255181.1:p.Gln2066Pro
XM_005255125.3:c.5825A>C XP_005255182.1:p.Gln1942Pro
XM_006720848.2:c.5981A>C XP_006720911.1:p.Gln1994Pro
XM_011522380.1:c.6188A>C XP_011520682.1:p.Gln2063Pro
XM_011522381.1:c.5489A>C XP_011520683.1:p.Gln1830Pro
XM_005255124.4:c.6197A>C XP_005255181.1:p.Gln2066Pro
XM_005255125.4:c.5825A>C XP_005255182.1:p.Gln1942Pro
XM_006720848.3:c.5981A>C XP_006720911.1:p.Gln1994Pro
XM_011522381.2:c.5489A>C XP_011520683.1:p.Gln1830Pro
XM_017022944.1:c.6236A>C XP_016878433.1:p.Gln2079Pro
NM_004380.3:c.6242A>C MANE Select NP_004371.2:p.Gln2081Pro