Canonical Allele Identifier: CA394557829
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs2151312760

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3729870T>A , CM000678.2:g.3729870T>A GRCh38
NC_000016.9:g.3779871T>A , CM000678.1:g.3779871T>A GRCh37
NC_000016.8:g.3719872T>A NCBI36
NG_009873.1:g.155251A>T
NG_009873.2:g.155844A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.5177A>T MANE Select ENSP00000262367.5:p.Tyr1726Phe
ENST00000262367.9:c.5177A>T ENSP00000262367.5:p.Tyr1726Phe
ENST00000382070.7:c.5063A>T ENSP00000371502.3:p.Tyr1688Phe
NM_001079846.1:c.5063A>T NP_001073315.1:p.Tyr1688Phe
NM_004380.2:c.5177A>T NP_004371.2:p.Tyr1726Phe
XM_005255124.3:c.5132A>T XP_005255181.1:p.Tyr1711Phe
XM_005255125.3:c.4760A>T XP_005255182.1:p.Tyr1587Phe
XM_006720848.2:c.4916A>T XP_006720911.1:p.Tyr1639Phe
XM_011522380.1:c.5123A>T XP_011520682.1:p.Tyr1708Phe
XM_011522381.1:c.4424A>T XP_011520683.1:p.Tyr1475Phe
XM_005255124.4:c.5132A>T XP_005255181.1:p.Tyr1711Phe
XM_005255125.4:c.4760A>T XP_005255182.1:p.Tyr1587Phe
XM_006720848.3:c.4916A>T XP_006720911.1:p.Tyr1639Phe
XM_011522381.2:c.4424A>T XP_011520683.1:p.Tyr1475Phe
XM_017022944.1:c.5171A>T XP_016878433.1:p.Tyr1724Phe
NM_004380.3:c.5177A>T MANE Select NP_004371.2:p.Tyr1726Phe