Canonical Allele Identifier: CA394563806
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs2151329734

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3736747G>A , CM000678.2:g.3736747G>A GRCh38
NC_000016.9:g.3786748G>A , CM000678.1:g.3786748G>A GRCh37
NC_000016.8:g.3726749G>A NCBI36
NG_009873.1:g.148374C>T
NG_009873.2:g.148967C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.4463C>T MANE Select ENSP00000262367.5:p.Pro1488Leu
ENST00000262367.9:c.4463C>T ENSP00000262367.5:p.Pro1488Leu
ENST00000382070.7:c.4349C>T ENSP00000371502.3:p.Pro1450Leu
ENST00000570939.2:c.3098C>T ENSP00000461002.2:p.Pro1033Leu
ENST00000571763.5:n.253C>T
ENST00000574740.1:n.284C>T
ENST00000576720.1:n.3286C>T
NM_001079846.1:c.4349C>T NP_001073315.1:p.Pro1450Leu
NM_004380.2:c.4463C>T NP_004371.2:p.Pro1488Leu
XM_005255124.3:c.4418C>T XP_005255181.1:p.Pro1473Leu
XM_005255125.3:c.4046C>T XP_005255182.1:p.Pro1349Leu
XM_006720848.2:c.4202C>T XP_006720911.1:p.Pro1401Leu
XM_011522380.1:c.4409C>T XP_011520682.1:p.Pro1470Leu
XM_011522381.1:c.3710C>T XP_011520683.1:p.Pro1237Leu
XM_005255124.4:c.4418C>T XP_005255181.1:p.Pro1473Leu
XM_005255125.4:c.4046C>T XP_005255182.1:p.Pro1349Leu
XM_006720848.3:c.4202C>T XP_006720911.1:p.Pro1401Leu
XM_011522381.2:c.3710C>T XP_011520683.1:p.Pro1237Leu
XM_017022944.1:c.4457C>T XP_016878433.1:p.Pro1486Leu
NM_004380.3:c.4463C>T MANE Select NP_004371.2:p.Pro1488Leu