Canonical Allele Identifier: CA2202928874
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3728847A= , CM000678.2:g.3728847A= GRCh38
NC_000016.9:g.3778848A= , CM000678.1:g.3778848A= GRCh37
NC_000016.8:g.3718849A= NCBI36
NG_009873.1:g.156274T=
NG_009873.2:g.156867T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.6200T= MANE Select ENSP00000262367.5:p.Leu2067=
ENST00000262367.9:c.6200T= ENSP00000262367.5:p.Leu2067=
ENST00000382070.7:c.6086T= ENSP00000371502.3:p.Leu2029=
NM_001079846.1:c.6086T= NP_001073315.1:p.Leu2029=
NM_004380.2:c.6200T= NP_004371.2:p.Leu2067=
XM_005255124.3:c.6155T= XP_005255181.1:p.Leu2052=
XM_005255125.3:c.5783T= XP_005255182.1:p.Leu1928=
XM_006720848.2:c.5939T= XP_006720911.1:p.Leu1980=
XM_011522380.1:c.6146T= XP_011520682.1:p.Leu2049=
XM_011522381.1:c.5447T= XP_011520683.1:p.Leu1816=
XM_005255124.4:c.6155T= XP_005255181.1:p.Leu2052=
XM_005255125.4:c.5783T= XP_005255182.1:p.Leu1928=
XM_006720848.3:c.5939T= XP_006720911.1:p.Leu1980=
XM_011522381.2:c.5447T= XP_011520683.1:p.Leu1816=
XM_017022944.1:c.6194T= XP_016878433.1:p.Leu2065=
NM_004380.3:c.6200T= MANE Select NP_004371.2:p.Leu2067=