Canonical Allele Identifier: CA493279159
Gene: CREBBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.3786671G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3736670G>T , CM000678.2:g.3736670G>T GRCh38
NC_000016.9:g.3786671G>T , CM000678.1:g.3786671G>T GRCh37
NC_000016.8:g.3726672G>T NCBI36
NG_009873.1:g.148451C>A
NG_009873.2:g.149044C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.4540C>A MANE Select ENSP00000262367.5:p.Arg1514=
ENST00000262367.9:c.4540C>A ENSP00000262367.5:p.Arg1514=
ENST00000382070.7:c.4426C>A ENSP00000371502.3:p.Arg1476=
ENST00000570939.2:c.3175C>A ENSP00000461002.2:p.Arg1059=
ENST00000571763.5:n.330C>A
ENST00000574740.1:n.361C>A
ENST00000576720.1:n.3363C>A
NM_001079846.1:c.4426C>A NP_001073315.1:p.Arg1476=
NM_004380.2:c.4540C>A NP_004371.2:p.Arg1514=
XM_005255124.3:c.4495C>A XP_005255181.1:p.Arg1499=
XM_005255125.3:c.4123C>A XP_005255182.1:p.Arg1375=
XM_006720848.2:c.4279C>A XP_006720911.1:p.Arg1427=
XM_011522380.1:c.4486C>A XP_011520682.1:p.Arg1496=
XM_011522381.1:c.3787C>A XP_011520683.1:p.Arg1263=
XM_005255124.4:c.4495C>A XP_005255181.1:p.Arg1499=
XM_005255125.4:c.4123C>A XP_005255182.1:p.Arg1375=
XM_006720848.3:c.4279C>A XP_006720911.1:p.Arg1427=
XM_011522381.2:c.3787C>A XP_011520683.1:p.Arg1263=
XM_017022944.1:c.4534C>A XP_016878433.1:p.Arg1512=
NM_004380.3:c.4540C>A MANE Select NP_004371.2:p.Arg1514=