Canonical Allele Identifier: CA394555756
Community Standard Title: NM_004380.3(CREBBP):c.5683C>T (p.Gln1895Ter)
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3729364G>A , CM000678.2:g.3729364G>A GRCh38
NC_000016.9:g.3779365G>A , CM000678.1:g.3779365G>A GRCh37
NC_000016.8:g.3719366G>A NCBI36
NG_009873.1:g.155757C>T
NG_009873.2:g.156350C>T

Transcript Alleles

HGVS Amino-acid Change
NM_004380.3:c.5683C>T MANE Select NP_004371.2:p.Gln1895Ter
ENST00000262367.10:c.5683C>T MANE Select ENSP00000262367.5:p.Gln1895Ter
NM_001079846.1:c.5569C>T NP_001073315.1:p.Gln1857Ter
NM_004380.2:c.5683C>T NP_004371.2:p.Gln1895Ter
ENST00000262367.9:c.5683C>T ENSP00000262367.5:p.Gln1895Ter
ENST00000382070.7:c.5569C>T ENSP00000371502.3:p.Gln1857Ter
XM_005255124.3:c.5638C>T XP_005255181.1:p.Gln1880Ter
XM_005255124.4:c.5638C>T XP_005255181.1:p.Gln1880Ter
XM_005255125.3:c.5266C>T XP_005255182.1:p.Gln1756Ter
XM_005255125.4:c.5266C>T XP_005255182.1:p.Gln1756Ter
XM_006720848.2:c.5422C>T XP_006720911.1:p.Gln1808Ter
XM_006720848.3:c.5422C>T XP_006720911.1:p.Gln1808Ter
XM_011522380.1:c.5629C>T XP_011520682.1:p.Gln1877Ter
XM_011522381.1:c.4930C>T XP_011520683.1:p.Gln1644Ter
XM_011522381.2:c.4930C>T XP_011520683.1:p.Gln1644Ter
XM_017022944.1:c.5677C>T XP_016878433.1:p.Gln1893Ter