Canonical Allele Identifier: CA493395109
Gene: CREBBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.3820859A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3770858A>C , CM000678.2:g.3770858A>C GRCh38
NC_000016.9:g.3820859A>C , CM000678.1:g.3820859A>C GRCh37
NC_000016.8:g.3760860A>C NCBI36
NG_009873.1:g.114263T>G
NG_009873.2:g.114856T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.2592T>G MANE Select ENSP00000262367.5:p.Ala864=
ENST00000262367.9:c.2592T>G ENSP00000262367.5:p.Ala864=
ENST00000382070.7:c.2478T>G ENSP00000371502.3:p.Ala826=
ENST00000570939.2:c.1197T>G ENSP00000461002.2:p.Ala399=
NM_001079846.1:c.2478T>G NP_001073315.1:p.Ala826=
NM_004380.2:c.2592T>G NP_004371.2:p.Ala864=
XM_005255124.3:c.2547T>G XP_005255181.1:p.Ala849=
XM_005255125.3:c.2464-1505T>G XP_005255182.1:n.2464-1505T>G
XM_006720848.2:c.2592T>G XP_006720911.1:p.Ala864=
XM_011522380.1:c.2538T>G XP_011520682.1:p.Ala846=
XM_011522381.1:c.1839T>G XP_011520683.1:p.Ala613=
XM_011522382.1:c.2592T>G XP_011520684.1:p.Ala864=
XM_005255124.4:c.2547T>G XP_005255181.1:p.Ala849=
XM_005255125.4:c.2464-1505T>G XP_005255182.1:n.2464-1505T>G
XM_006720848.3:c.2592T>G XP_006720911.1:p.Ala864=
XM_011522381.2:c.1839T>G XP_011520683.1:p.Ala613=
XM_011522382.3:c.2592T>G XP_011520684.1:p.Ala864=
XM_017022944.1:c.2586T>G XP_016878433.1:p.Ala862=
NM_004380.3:c.2592T>G MANE Select NP_004371.2:p.Ala864=