Canonical Allele Identifier: CA394557225
Gene: CREBBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3729735C>A , CM000678.2:g.3729735C>A GRCh38
NC_000016.9:g.3779736C>A , CM000678.1:g.3779736C>A GRCh37
NC_000016.8:g.3719737C>A NCBI36
NG_009873.1:g.155386G>T
NG_009873.2:g.155979G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.5312G>T MANE Select ENSP00000262367.5:p.Ser1771Ile
ENST00000262367.9:c.5312G>T ENSP00000262367.5:p.Ser1771Ile
ENST00000382070.7:c.5198G>T ENSP00000371502.3:p.Ser1733Ile
NM_001079846.1:c.5198G>T NP_001073315.1:p.Ser1733Ile
NM_004380.2:c.5312G>T NP_004371.2:p.Ser1771Ile
XM_005255124.3:c.5267G>T XP_005255181.1:p.Ser1756Ile
XM_005255125.3:c.4895G>T XP_005255182.1:p.Ser1632Ile
XM_006720848.2:c.5051G>T XP_006720911.1:p.Ser1684Ile
XM_011522380.1:c.5258G>T XP_011520682.1:p.Ser1753Ile
XM_011522381.1:c.4559G>T XP_011520683.1:p.Ser1520Ile
XM_005255124.4:c.5267G>T XP_005255181.1:p.Ser1756Ile
XM_005255125.4:c.4895G>T XP_005255182.1:p.Ser1632Ile
XM_006720848.3:c.5051G>T XP_006720911.1:p.Ser1684Ile
XM_011522381.2:c.4559G>T XP_011520683.1:p.Ser1520Ile
XM_017022944.1:c.5306G>T XP_016878433.1:p.Ser1769Ile
NM_004380.3:c.5312G>T MANE Select NP_004371.2:p.Ser1771Ile