Canonical Allele Identifier: CA394553884
Gene: CREBBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3728835A>G , CM000678.2:g.3728835A>G GRCh38
NC_000016.9:g.3778836A>G , CM000678.1:g.3778836A>G GRCh37
NC_000016.8:g.3718837A>G NCBI36
NG_009873.1:g.156286T>C
NG_009873.2:g.156879T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.6212T>C MANE Select ENSP00000262367.5:p.Leu2071Pro
ENST00000262367.9:c.6212T>C ENSP00000262367.5:p.Leu2071Pro
ENST00000382070.7:c.6098T>C ENSP00000371502.3:p.Leu2033Pro
NM_001079846.1:c.6098T>C NP_001073315.1:p.Leu2033Pro
NM_004380.2:c.6212T>C NP_004371.2:p.Leu2071Pro
XM_005255124.3:c.6167T>C XP_005255181.1:p.Leu2056Pro
XM_005255125.3:c.5795T>C XP_005255182.1:p.Leu1932Pro
XM_006720848.2:c.5951T>C XP_006720911.1:p.Leu1984Pro
XM_011522380.1:c.6158T>C XP_011520682.1:p.Leu2053Pro
XM_011522381.1:c.5459T>C XP_011520683.1:p.Leu1820Pro
XM_005255124.4:c.6167T>C XP_005255181.1:p.Leu2056Pro
XM_005255125.4:c.5795T>C XP_005255182.1:p.Leu1932Pro
XM_006720848.3:c.5951T>C XP_006720911.1:p.Leu1984Pro
XM_011522381.2:c.5459T>C XP_011520683.1:p.Leu1820Pro
XM_017022944.1:c.6206T>C XP_016878433.1:p.Leu2069Pro
NM_004380.3:c.6212T>C MANE Select NP_004371.2:p.Leu2071Pro