Canonical Allele Identifier: CA394553893
Gene: CREBBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3728840G>C , CM000678.2:g.3728840G>C GRCh38
NC_000016.9:g.3778841G>C , CM000678.1:g.3778841G>C GRCh37
NC_000016.8:g.3718842G>C NCBI36
NG_009873.1:g.156281C>G
NG_009873.2:g.156874C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.6207C>G MANE Select ENSP00000262367.5:p.Asp2069Glu
ENST00000262367.9:c.6207C>G ENSP00000262367.5:p.Asp2069Glu
ENST00000382070.7:c.6093C>G ENSP00000371502.3:p.Asp2031Glu
NM_001079846.1:c.6093C>G NP_001073315.1:p.Asp2031Glu
NM_004380.2:c.6207C>G NP_004371.2:p.Asp2069Glu
XM_005255124.3:c.6162C>G XP_005255181.1:p.Asp2054Glu
XM_005255125.3:c.5790C>G XP_005255182.1:p.Asp1930Glu
XM_006720848.2:c.5946C>G XP_006720911.1:p.Asp1982Glu
XM_011522380.1:c.6153C>G XP_011520682.1:p.Asp2051Glu
XM_011522381.1:c.5454C>G XP_011520683.1:p.Asp1818Glu
XM_005255124.4:c.6162C>G XP_005255181.1:p.Asp2054Glu
XM_005255125.4:c.5790C>G XP_005255182.1:p.Asp1930Glu
XM_006720848.3:c.5946C>G XP_006720911.1:p.Asp1982Glu
XM_011522381.2:c.5454C>G XP_011520683.1:p.Asp1818Glu
XM_017022944.1:c.6201C>G XP_016878433.1:p.Asp2067Glu
NM_004380.3:c.6207C>G MANE Select NP_004371.2:p.Asp2069Glu