Canonical Allele Identifier: CA394556029
Gene: CREBBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3729492T>A , CM000678.2:g.3729492T>A GRCh38
NC_000016.9:g.3779493T>A , CM000678.1:g.3779493T>A GRCh37
NC_000016.8:g.3719494T>A NCBI36
NG_009873.1:g.155629A>T
NG_009873.2:g.156222A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.5555A>T MANE Select ENSP00000262367.5:p.Gln1852Leu
ENST00000262367.9:c.5555A>T ENSP00000262367.5:p.Gln1852Leu
ENST00000382070.7:c.5441A>T ENSP00000371502.3:p.Gln1814Leu
NM_001079846.1:c.5441A>T NP_001073315.1:p.Gln1814Leu
NM_004380.2:c.5555A>T NP_004371.2:p.Gln1852Leu
XM_005255124.3:c.5510A>T XP_005255181.1:p.Gln1837Leu
XM_005255125.3:c.5138A>T XP_005255182.1:p.Gln1713Leu
XM_006720848.2:c.5294A>T XP_006720911.1:p.Gln1765Leu
XM_011522380.1:c.5501A>T XP_011520682.1:p.Gln1834Leu
XM_011522381.1:c.4802A>T XP_011520683.1:p.Gln1601Leu
XM_005255124.4:c.5510A>T XP_005255181.1:p.Gln1837Leu
XM_005255125.4:c.5138A>T XP_005255182.1:p.Gln1713Leu
XM_006720848.3:c.5294A>T XP_006720911.1:p.Gln1765Leu
XM_011522381.2:c.4802A>T XP_011520683.1:p.Gln1601Leu
XM_017022944.1:c.5549A>T XP_016878433.1:p.Gln1850Leu
NM_004380.3:c.5555A>T MANE Select NP_004371.2:p.Gln1852Leu