Canonical Allele Identifier: CA2202940830
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3740448C= , CM000678.2:g.3740448C= GRCh38
NC_000016.9:g.3790449C= , CM000678.1:g.3790449C= GRCh37
NC_000016.8:g.3730450C= NCBI36
NG_009873.1:g.144673G=
NG_009873.2:g.145266G=

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.4084G= MANE Select ENSP00000262367.5:p.Val1362=
ENST00000262367.9:c.4084G= ENSP00000262367.5:p.Val1362=
ENST00000382070.7:c.3970G= ENSP00000371502.3:p.Val1324=
ENST00000570939.2:c.2719G= ENSP00000461002.2:p.Val907=
ENST00000572569.1:n.548G=
ENST00000573517.6:c.390G=
ENST00000574740.1:n.166G=
ENST00000576720.1:n.3021G=
NM_001079846.1:c.3970G= NP_001073315.1:p.Val1324=
NM_004380.2:c.4084G= NP_004371.2:p.Val1362=
XM_005255124.3:c.4039G= XP_005255181.1:p.Val1347=
XM_005255125.3:c.3667G= XP_005255182.1:p.Val1223=
XM_006720848.2:c.4084G= XP_006720911.1:p.Val1362=
XM_011522380.1:c.4030G= XP_011520682.1:p.Val1344=
XM_011522381.1:c.3331G= XP_011520683.1:p.Val1111=
XM_005255124.4:c.4039G= XP_005255181.1:p.Val1347=
XM_005255125.4:c.3667G= XP_005255182.1:p.Val1223=
XM_006720848.3:c.4084G= XP_006720911.1:p.Val1362=
XM_011522381.2:c.3331G= XP_011520683.1:p.Val1111=
XM_017022944.1:c.4078G= XP_016878433.1:p.Val1360=
NM_004380.3:c.4084G= MANE Select NP_004371.2:p.Val1362=