Canonical Allele Identifier: CA394553787
Gene: CREBBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3728791C>G , CM000678.2:g.3728791C>G GRCh38
NC_000016.9:g.3778792C>G , CM000678.1:g.3778792C>G GRCh37
NC_000016.8:g.3718793C>G NCBI36
NG_009873.1:g.156330G>C
NG_009873.2:g.156923G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.6256G>C MANE Select ENSP00000262367.5:p.Val2086Leu
ENST00000262367.9:c.6256G>C ENSP00000262367.5:p.Val2086Leu
ENST00000382070.7:c.6142G>C ENSP00000371502.3:p.Val2048Leu
NM_001079846.1:c.6142G>C NP_001073315.1:p.Val2048Leu
NM_004380.2:c.6256G>C NP_004371.2:p.Val2086Leu
XM_005255124.3:c.6211G>C XP_005255181.1:p.Val2071Leu
XM_005255125.3:c.5839G>C XP_005255182.1:p.Val1947Leu
XM_006720848.2:c.5995G>C XP_006720911.1:p.Val1999Leu
XM_011522380.1:c.6202G>C XP_011520682.1:p.Val2068Leu
XM_011522381.1:c.5503G>C XP_011520683.1:p.Val1835Leu
XM_005255124.4:c.6211G>C XP_005255181.1:p.Val2071Leu
XM_005255125.4:c.5839G>C XP_005255182.1:p.Val1947Leu
XM_006720848.3:c.5995G>C XP_006720911.1:p.Val1999Leu
XM_011522381.2:c.5503G>C XP_011520683.1:p.Val1835Leu
XM_017022944.1:c.6250G>C XP_016878433.1:p.Val2084Leu
NM_004380.3:c.6256G>C MANE Select NP_004371.2:p.Val2086Leu