Canonical Allele Identifier: CA394565293
Gene: CREBBP HGNC NCBI

Linked Data

gnomAD v4: 16-3740442-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3740442T>G , CM000678.2:g.3740442T>G GRCh38
NC_000016.9:g.3790443T>G , CM000678.1:g.3790443T>G GRCh37
NC_000016.8:g.3730444T>G NCBI36
NG_009873.1:g.144679A>C
NG_009873.2:g.145272A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.4090A>C MANE Select ENSP00000262367.5:p.Ser1364Arg
ENST00000262367.9:c.4090A>C ENSP00000262367.5:p.Ser1364Arg
ENST00000382070.7:c.3976A>C ENSP00000371502.3:p.Ser1326Arg
ENST00000570939.2:c.2725A>C ENSP00000461002.2:p.Ser909Arg
ENST00000573517.6:c.396A>C
ENST00000574740.1:n.172A>C
ENST00000576720.1:n.3027A>C
NM_001079846.1:c.3976A>C NP_001073315.1:p.Ser1326Arg
NM_004380.2:c.4090A>C NP_004371.2:p.Ser1364Arg
XM_005255124.3:c.4045A>C XP_005255181.1:p.Ser1349Arg
XM_005255125.3:c.3673A>C XP_005255182.1:p.Ser1225Arg
XM_006720848.2:c.4090A>C XP_006720911.1:p.Ser1364Arg
XM_011522380.1:c.4036A>C XP_011520682.1:p.Ser1346Arg
XM_011522381.1:c.3337A>C XP_011520683.1:p.Ser1113Arg
XM_005255124.4:c.4045A>C XP_005255181.1:p.Ser1349Arg
XM_005255125.4:c.3673A>C XP_005255182.1:p.Ser1225Arg
XM_006720848.3:c.4090A>C XP_006720911.1:p.Ser1364Arg
XM_011522381.2:c.3337A>C XP_011520683.1:p.Ser1113Arg
XM_017022944.1:c.4084A>C XP_016878433.1:p.Ser1362Arg
NM_004380.3:c.4090A>C MANE Select NP_004371.2:p.Ser1364Arg