Canonical Allele Identifier: CA493280354
Gene: CREBBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.3790453T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3740452T>G , CM000678.2:g.3740452T>G GRCh38
NC_000016.9:g.3790453T>G , CM000678.1:g.3790453T>G GRCh37
NC_000016.8:g.3730454T>G NCBI36
NG_009873.1:g.144669A>C
NG_009873.2:g.145262A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.4080A>C MANE Select ENSP00000262367.5:p.Arg1360=
ENST00000262367.9:c.4080A>C ENSP00000262367.5:p.Arg1360=
ENST00000382070.7:c.3966A>C ENSP00000371502.3:p.Arg1322=
ENST00000570939.2:c.2715A>C ENSP00000461002.2:p.Arg905=
ENST00000572569.1:n.544A>C
ENST00000573517.6:c.386A>C
ENST00000574740.1:n.162A>C
ENST00000576720.1:n.3017A>C
NM_001079846.1:c.3966A>C NP_001073315.1:p.Arg1322=
NM_004380.2:c.4080A>C NP_004371.2:p.Arg1360=
XM_005255124.3:c.4035A>C XP_005255181.1:p.Arg1345=
XM_005255125.3:c.3663A>C XP_005255182.1:p.Arg1221=
XM_006720848.2:c.4080A>C XP_006720911.1:p.Arg1360=
XM_011522380.1:c.4026A>C XP_011520682.1:p.Arg1342=
XM_011522381.1:c.3327A>C XP_011520683.1:p.Arg1109=
XM_005255124.4:c.4035A>C XP_005255181.1:p.Arg1345=
XM_005255125.4:c.3663A>C XP_005255182.1:p.Arg1221=
XM_006720848.3:c.4080A>C XP_006720911.1:p.Arg1360=
XM_011522381.2:c.3327A>C XP_011520683.1:p.Arg1109=
XM_017022944.1:c.4074A>C XP_016878433.1:p.Arg1358=
NM_004380.3:c.4080A>C MANE Select NP_004371.2:p.Arg1360=