Canonical Allele Identifier: CA394554948
Gene: CREBBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3729118T>A , CM000678.2:g.3729118T>A GRCh38
NC_000016.9:g.3779119T>A , CM000678.1:g.3779119T>A GRCh37
NC_000016.8:g.3719120T>A NCBI36
NG_009873.1:g.156003A>T
NG_009873.2:g.156596A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.5929A>T MANE Select ENSP00000262367.5:p.Ile1977Phe
ENST00000262367.9:c.5929A>T ENSP00000262367.5:p.Ile1977Phe
ENST00000382070.7:c.5815A>T ENSP00000371502.3:p.Ile1939Phe
NM_001079846.1:c.5815A>T NP_001073315.1:p.Ile1939Phe
NM_004380.2:c.5929A>T NP_004371.2:p.Ile1977Phe
XM_005255124.3:c.5884A>T XP_005255181.1:p.Ile1962Phe
XM_005255125.3:c.5512A>T XP_005255182.1:p.Ile1838Phe
XM_006720848.2:c.5668A>T XP_006720911.1:p.Ile1890Phe
XM_011522380.1:c.5875A>T XP_011520682.1:p.Ile1959Phe
XM_011522381.1:c.5176A>T XP_011520683.1:p.Ile1726Phe
XM_005255124.4:c.5884A>T XP_005255181.1:p.Ile1962Phe
XM_005255125.4:c.5512A>T XP_005255182.1:p.Ile1838Phe
XM_006720848.3:c.5668A>T XP_006720911.1:p.Ile1890Phe
XM_011522381.2:c.5176A>T XP_011520683.1:p.Ile1726Phe
XM_017022944.1:c.5923A>T XP_016878433.1:p.Ile1975Phe
NM_004380.3:c.5929A>T MANE Select NP_004371.2:p.Ile1977Phe