Canonical Allele Identifier: CA2229208893
Gene: HSF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67165732G= , CM000678.2:g.67165732G= GRCh38
NC_000016.9:g.67199635G= , CM000678.1:g.67199635G= GRCh37
NC_000016.8:g.65757136G= NCBI36
NG_009294.1:g.7348G=
NG_029566.1:g.231G=

Transcript Alleles

HGVS Amino-acid change
ENST00000517867.2:n.529G=
ENST00000523077.2:n.745G=
ENST00000521374.6:c.246G= MANE Select ENSP00000430947.2:p.Lys82=
ENST00000434833.6:c.246G= ENSP00000403219.2:p.Lys82=
ENST00000517685.5:c.246G= ENSP00000428978.1:p.Lys82=
ENST00000517729.5:c.120G= ENSP00000430299.1:p.Lys40=
ENST00000518753.5:c.418G=
ENST00000521314.5:c.137G= ENSP00000429580.1:p.Arg46=
ENST00000521374.5:c.246G= ENSP00000430947.1:p.Lys82=
ENST00000521624.5:c.246G= ENSP00000428161.1:p.Lys82=
ENST00000522023.1:n.313G=
ENST00000522295.5:c.246G= ENSP00000427832.1:p.Lys82=
ENST00000522870.5:n.465G=
ENST00000523077.1:n.745G=
ENST00000523562.5:c.246G= ENSP00000430631.1:p.Lys82=
ENST00000580114.5:c.1211G=
ENST00000584272.5:c.246G= ENSP00000463706.1:p.Lys82=
NM_001040667.2:c.246G= NP_001035757.1:p.Lys82=
NM_001538.3:c.246G= NP_001529.2:p.Lys82=
NM_001040667.3:c.246G= NP_001035757.1:p.Lys82=
NM_001374674.1:c.246G= NP_001361603.1:p.Lys82=
NM_001374675.1:c.246G= MANE Select NP_001361604.1:p.Lys82=
NM_001538.4:c.246G= NP_001529.2:p.Lys82=