Canonical Allele Identifier: CA394554379
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs2151306389

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3728982T>A , CM000678.2:g.3728982T>A GRCh38
NC_000016.9:g.3778983T>A , CM000678.1:g.3778983T>A GRCh37
NC_000016.8:g.3718984T>A NCBI36
NG_009873.1:g.156139A>T
NG_009873.2:g.156732A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.6065A>T MANE Select ENSP00000262367.5:p.Gln2022Leu
ENST00000262367.9:c.6065A>T ENSP00000262367.5:p.Gln2022Leu
ENST00000382070.7:c.5951A>T ENSP00000371502.3:p.Gln1984Leu
NM_001079846.1:c.5951A>T NP_001073315.1:p.Gln1984Leu
NM_004380.2:c.6065A>T NP_004371.2:p.Gln2022Leu
XM_005255124.3:c.6020A>T XP_005255181.1:p.Gln2007Leu
XM_005255125.3:c.5648A>T XP_005255182.1:p.Gln1883Leu
XM_006720848.2:c.5804A>T XP_006720911.1:p.Gln1935Leu
XM_011522380.1:c.6011A>T XP_011520682.1:p.Gln2004Leu
XM_011522381.1:c.5312A>T XP_011520683.1:p.Gln1771Leu
XM_005255124.4:c.6020A>T XP_005255181.1:p.Gln2007Leu
XM_005255125.4:c.5648A>T XP_005255182.1:p.Gln1883Leu
XM_006720848.3:c.5804A>T XP_006720911.1:p.Gln1935Leu
XM_011522381.2:c.5312A>T XP_011520683.1:p.Gln1771Leu
XM_017022944.1:c.6059A>T XP_016878433.1:p.Gln2020Leu
NM_004380.3:c.6065A>T MANE Select NP_004371.2:p.Gln2022Leu