Canonical Allele Identifier: CA394555039
Community Standard Title: NM_004380.3(CREBBP):c.5902C>T (p.Gln1968Ter)
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3729145G>A , CM000678.2:g.3729145G>A GRCh38
NC_000016.9:g.3779146G>A , CM000678.1:g.3779146G>A GRCh37
NC_000016.8:g.3719147G>A NCBI36
NG_009873.1:g.155976C>T
NG_009873.2:g.156569C>T

Transcript Alleles

HGVS Amino-acid Change
NM_004380.3:c.5902C>T MANE Select NP_004371.2:p.Gln1968Ter
ENST00000262367.10:c.5902C>T MANE Select ENSP00000262367.5:p.Gln1968Ter
NM_001079846.1:c.5788C>T NP_001073315.1:p.Gln1930Ter
NM_004380.2:c.5902C>T NP_004371.2:p.Gln1968Ter
ENST00000262367.9:c.5902C>T ENSP00000262367.5:p.Gln1968Ter
ENST00000382070.7:c.5788C>T ENSP00000371502.3:p.Gln1930Ter
XM_005255124.3:c.5857C>T XP_005255181.1:p.Gln1953Ter
XM_005255124.4:c.5857C>T XP_005255181.1:p.Gln1953Ter
XM_005255125.3:c.5485C>T XP_005255182.1:p.Gln1829Ter
XM_005255125.4:c.5485C>T XP_005255182.1:p.Gln1829Ter
XM_006720848.2:c.5641C>T XP_006720911.1:p.Gln1881Ter
XM_006720848.3:c.5641C>T XP_006720911.1:p.Gln1881Ter
XM_011522380.1:c.5848C>T XP_011520682.1:p.Gln1950Ter
XM_011522381.1:c.5149C>T XP_011520683.1:p.Gln1717Ter
XM_011522381.2:c.5149C>T XP_011520683.1:p.Gln1717Ter
XM_017022944.1:c.5896C>T XP_016878433.1:p.Gln1966Ter