Canonical Allele Identifier: CA493277670
Gene: CREBBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.3860754T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3810753T>A , CM000678.2:g.3810753T>A GRCh38
NC_000016.9:g.3860754T>A , CM000678.1:g.3860754T>A GRCh37
NC_000016.8:g.3800755T>A NCBI36
NG_009873.1:g.74368A>T
NG_009873.2:g.74961A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.825A>T MANE Select ENSP00000262367.5:p.Pro275=
ENST00000635899.1:n.67A>T
ENST00000262367.9:c.825A>T ENSP00000262367.5:p.Pro275=
ENST00000382070.7:c.825A>T ENSP00000371502.3:p.Pro275=
NM_001079846.1:c.825A>T NP_001073315.1:p.Pro275=
NM_004380.2:c.825A>T NP_004371.2:p.Pro275=
XM_005255124.3:c.825A>T XP_005255181.1:p.Pro275=
XM_005255125.3:c.825A>T XP_005255182.1:p.Pro275=
XM_006720848.2:c.825A>T XP_006720911.1:p.Pro275=
XM_011522380.1:c.771A>T XP_011520682.1:p.Pro257=
XM_011522381.1:c.72A>T XP_011520683.1:p.Pro24=
XM_011522382.1:c.825A>T XP_011520684.1:p.Pro275=
XM_005255124.4:c.825A>T XP_005255181.1:p.Pro275=
XM_005255125.4:c.825A>T XP_005255182.1:p.Pro275=
XM_006720848.3:c.825A>T XP_006720911.1:p.Pro275=
XM_011522381.2:c.72A>T XP_011520683.1:p.Pro24=
XM_011522382.3:c.825A>T XP_011520684.1:p.Pro275=
XM_017022944.1:c.825A>T XP_016878433.1:p.Pro275=
NM_004380.3:c.825A>T MANE Select NP_004371.2:p.Pro275=