Canonical Allele Identifier: CA396264575
Gene: HSF4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67165838C>G , CM000678.2:g.67165838C>G GRCh38
NC_000016.9:g.67199741C>G , CM000678.1:g.67199741C>G GRCh37
NC_000016.8:g.65757242C>G NCBI36
NG_009294.1:g.7454C>G
NG_029566.1:g.337C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000517867.2:n.635C>G
ENST00000523077.2:n.851C>G
ENST00000521374.6:c.352C>G MANE Select ENSP00000430947.2:p.Arg118Gly
ENST00000434833.6:c.352C>G ENSP00000403219.2:p.Arg118Gly
ENST00000517685.5:c.352C>G ENSP00000428978.1:p.Arg118Gly
ENST00000517729.5:c.226C>G ENSP00000430299.1:p.Arg76Gly
ENST00000521314.5:c.*99C>G ENSP00000429580.1:n.*99C>G
ENST00000521374.5:c.352C>G ENSP00000430947.1:p.Arg118Gly
ENST00000521624.5:c.352C>G ENSP00000428161.1:p.Arg118Gly
ENST00000522023.1:n.419C>G
ENST00000522295.5:c.352C>G ENSP00000427832.1:p.Arg118Gly
ENST00000522870.5:n.571C>G
ENST00000523562.5:c.352C>G ENSP00000430631.1:p.Arg118Gly
ENST00000584272.5:c.352C>G ENSP00000463706.1:p.Arg118Gly
NM_001040667.2:c.352C>G NP_001035757.1:p.Arg118Gly
NM_001538.3:c.352C>G NP_001529.2:p.Arg118Gly
NM_001040667.3:c.352C>G NP_001035757.1:p.Arg118Gly
NM_001374674.1:c.352C>G NP_001361603.1:p.Arg118Gly
NM_001374675.1:c.352C>G MANE Select NP_001361604.1:p.Arg118Gly
NM_001538.4:c.352C>G NP_001529.2:p.Arg118Gly