Canonical Allele Identifier: CA396264489
Gene: HSF4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67165829G>C , CM000678.2:g.67165829G>C GRCh38
NC_000016.9:g.67199732G>C , CM000678.1:g.67199732G>C GRCh37
NC_000016.8:g.65757233G>C NCBI36
NG_009294.1:g.7445G>C
NG_029566.1:g.328G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000517867.2:n.626G>C
ENST00000523077.2:n.842G>C
ENST00000521374.6:c.343G>C MANE Select ENSP00000430947.2:p.Glu115Gln
ENST00000434833.6:c.343G>C ENSP00000403219.2:p.Glu115Gln
ENST00000517685.5:c.343G>C ENSP00000428978.1:p.Glu115Gln
ENST00000517729.5:c.217G>C ENSP00000430299.1:p.Glu73Gln
ENST00000521314.5:c.*90G>C ENSP00000429580.1:n.*90G>C
ENST00000521374.5:c.343G>C ENSP00000430947.1:p.Glu115Gln
ENST00000521624.5:c.343G>C ENSP00000428161.1:p.Glu115Gln
ENST00000522023.1:n.410G>C
ENST00000522295.5:c.343G>C ENSP00000427832.1:p.Glu115Gln
ENST00000522870.5:n.562G>C
ENST00000523562.5:c.343G>C ENSP00000430631.1:p.Glu115Gln
ENST00000584272.5:c.343G>C ENSP00000463706.1:p.Glu115Gln
NM_001040667.2:c.343G>C NP_001035757.1:p.Glu115Gln
NM_001538.3:c.343G>C NP_001529.2:p.Glu115Gln
NM_001040667.3:c.343G>C NP_001035757.1:p.Glu115Gln
NM_001374674.1:c.343G>C NP_001361603.1:p.Glu115Gln
NM_001374675.1:c.343G>C MANE Select NP_001361604.1:p.Glu115Gln
NM_001538.4:c.343G>C NP_001529.2:p.Glu115Gln