Canonical Allele Identifier: CA394565290
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs2151340181

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3740441C>T , CM000678.2:g.3740441C>T GRCh38
NC_000016.9:g.3790442C>T , CM000678.1:g.3790442C>T GRCh37
NC_000016.8:g.3730443C>T NCBI36
NG_009873.1:g.144680G>A
NG_009873.2:g.145273G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.4091G>A MANE Select ENSP00000262367.5:p.Ser1364Asn
ENST00000262367.9:c.4091G>A ENSP00000262367.5:p.Ser1364Asn
ENST00000382070.7:c.3977G>A ENSP00000371502.3:p.Ser1326Asn
ENST00000570939.2:c.2726G>A ENSP00000461002.2:p.Ser909Asn
ENST00000573517.6:c.397G>A
ENST00000574740.1:n.173G>A
ENST00000576720.1:n.3028G>A
NM_001079846.1:c.3977G>A NP_001073315.1:p.Ser1326Asn
NM_004380.2:c.4091G>A NP_004371.2:p.Ser1364Asn
XM_005255124.3:c.4046G>A XP_005255181.1:p.Ser1349Asn
XM_005255125.3:c.3674G>A XP_005255182.1:p.Ser1225Asn
XM_006720848.2:c.4091G>A XP_006720911.1:p.Ser1364Asn
XM_011522380.1:c.4037G>A XP_011520682.1:p.Ser1346Asn
XM_011522381.1:c.3338G>A XP_011520683.1:p.Ser1113Asn
XM_005255124.4:c.4046G>A XP_005255181.1:p.Ser1349Asn
XM_005255125.4:c.3674G>A XP_005255182.1:p.Ser1225Asn
XM_006720848.3:c.4091G>A XP_006720911.1:p.Ser1364Asn
XM_011522381.2:c.3338G>A XP_011520683.1:p.Ser1113Asn
XM_017022944.1:c.4085G>A XP_016878433.1:p.Ser1362Asn
NM_004380.3:c.4091G>A MANE Select NP_004371.2:p.Ser1364Asn