Canonical Allele Identifier: CA8101769
Gene: HSF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 320179
dbSNP Id: rs367654370

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67165745G>A , CM000678.2:g.67165745G>A GRCh38
NC_000016.9:g.67199648G>A , CM000678.1:g.67199648G>A GRCh37
NC_000016.8:g.65757149G>A NCBI36
NG_009294.1:g.7361G>A
NG_029566.1:g.244G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000517867.2:n.542G>A
ENST00000523077.2:n.758G>A
ENST00000521374.6:c.259G>A MANE Select ENSP00000430947.2:p.Glu87Lys
ENST00000434833.6:c.259G>A ENSP00000403219.2:p.Glu87Lys
ENST00000517685.5:c.259G>A ENSP00000428978.1:p.Glu87Lys
ENST00000517729.5:c.133G>A ENSP00000430299.1:p.Glu45Lys
ENST00000518753.5:c.431G>A
ENST00000521314.5:c.*6G>A ENSP00000429580.1:n.*6G>A
ENST00000521374.5:c.259G>A ENSP00000430947.1:p.Glu87Lys
ENST00000521624.5:c.259G>A ENSP00000428161.1:p.Glu87Lys
ENST00000522023.1:n.326G>A
ENST00000522295.5:c.259G>A ENSP00000427832.1:p.Glu87Lys
ENST00000522870.5:n.478G>A
ENST00000523077.1:n.758G>A
ENST00000523562.5:c.259G>A ENSP00000430631.1:p.Glu87Lys
ENST00000580114.5:c.1224G>A
ENST00000584272.5:c.259G>A ENSP00000463706.1:p.Glu87Lys
NM_001040667.2:c.259G>A NP_001035757.1:p.Glu87Lys
NM_001538.3:c.259G>A NP_001529.2:p.Glu87Lys
NM_001040667.3:c.259G>A NP_001035757.1:p.Glu87Lys
NM_001374674.1:c.259G>A NP_001361603.1:p.Glu87Lys
NM_001374675.1:c.259G>A MANE Select NP_001361604.1:p.Glu87Lys
NM_001538.4:c.259G>A NP_001529.2:p.Glu87Lys