Canonical Allele Identifier: CA394550161
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs750047644

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3727770A>G , CM000678.2:g.3727770A>G GRCh38
NC_000016.9:g.3777771A>G , CM000678.1:g.3777771A>G GRCh37
NC_000016.8:g.3717772A>G NCBI36
NG_009873.1:g.157351T>C
NG_009873.2:g.157944T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.7277T>C MANE Select ENSP00000262367.5:p.Leu2426Pro
ENST00000262367.9:c.7277T>C ENSP00000262367.5:p.Leu2426Pro
ENST00000382070.7:c.7163T>C ENSP00000371502.3:p.Leu2388Pro
NM_001079846.1:c.7163T>C NP_001073315.1:p.Leu2388Pro
NM_004380.2:c.7277T>C NP_004371.2:p.Leu2426Pro
XM_005255124.3:c.7232T>C XP_005255181.1:p.Leu2411Pro
XM_005255125.3:c.6860T>C XP_005255182.1:p.Leu2287Pro
XM_006720848.2:c.7016T>C XP_006720911.1:p.Leu2339Pro
XM_011522380.1:c.7223T>C XP_011520682.1:p.Leu2408Pro
XM_011522381.1:c.6524T>C XP_011520683.1:p.Leu2175Pro
XM_005255124.4:c.7232T>C XP_005255181.1:p.Leu2411Pro
XM_005255125.4:c.6860T>C XP_005255182.1:p.Leu2287Pro
XM_006720848.3:c.7016T>C XP_006720911.1:p.Leu2339Pro
XM_011522381.2:c.6524T>C XP_011520683.1:p.Leu2175Pro
XM_017022944.1:c.7271T>C XP_016878433.1:p.Leu2424Pro
NM_004380.3:c.7277T>C MANE Select NP_004371.2:p.Leu2426Pro