Canonical Allele Identifier: CA2202928871
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3728839G= , CM000678.2:g.3728839G= GRCh38
NC_000016.9:g.3778840G= , CM000678.1:g.3778840G= GRCh37
NC_000016.8:g.3718841G= NCBI36
NG_009873.1:g.156282C=
NG_009873.2:g.156875C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.6208C= MANE Select ENSP00000262367.5:p.Leu2070=
ENST00000262367.9:c.6208C= ENSP00000262367.5:p.Leu2070=
ENST00000382070.7:c.6094C= ENSP00000371502.3:p.Leu2032=
NM_001079846.1:c.6094C= NP_001073315.1:p.Leu2032=
NM_004380.2:c.6208C= NP_004371.2:p.Leu2070=
XM_005255124.3:c.6163C= XP_005255181.1:p.Leu2055=
XM_005255125.3:c.5791C= XP_005255182.1:p.Leu1931=
XM_006720848.2:c.5947C= XP_006720911.1:p.Leu1983=
XM_011522380.1:c.6154C= XP_011520682.1:p.Leu2052=
XM_011522381.1:c.5455C= XP_011520683.1:p.Leu1819=
XM_005255124.4:c.6163C= XP_005255181.1:p.Leu2055=
XM_005255125.4:c.5791C= XP_005255182.1:p.Leu1931=
XM_006720848.3:c.5947C= XP_006720911.1:p.Leu1983=
XM_011522381.2:c.5455C= XP_011520683.1:p.Leu1819=
XM_017022944.1:c.6202C= XP_016878433.1:p.Leu2068=
NM_004380.3:c.6208C= MANE Select NP_004371.2:p.Leu2070=