Canonical Allele Identifier: CA8101678
Gene: HSF4 HGNC NCBI

Linked Data

dbSNP Id: rs781235789

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67164856C>T , CM000678.2:g.67164856C>T GRCh38
NC_000016.9:g.67198759C>T , CM000678.1:g.67198759C>T GRCh37
NC_000016.8:g.65756260C>T NCBI36
NG_009294.1:g.6472C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000521374.6:c.45C>T MANE Select ENSP00000430947.2:p.Ser15=
ENST00000434833.6:c.45C>T ENSP00000403219.2:p.Ser15=
ENST00000517685.5:c.45C>T ENSP00000428978.1:p.Ser15=
ENST00000518227.1:c.687C>T
ENST00000518753.5:c.296-666C>T
ENST00000521314.5:c.45C>T ENSP00000429580.1:p.Ser15=
ENST00000521374.5:c.45C>T ENSP00000430947.1:p.Ser15=
ENST00000521624.5:c.45C>T ENSP00000428161.1:p.Ser15=
ENST00000522023.1:n.112C>T
ENST00000522295.5:c.45C>T ENSP00000427832.1:p.Ser15=
ENST00000522870.5:n.176C>T
ENST00000523562.5:c.45C>T ENSP00000430631.1:p.Ser15=
ENST00000580114.5:c.1010C>T
ENST00000584272.5:c.45C>T ENSP00000463706.1:p.Ser15=
NM_001040667.2:c.45C>T NP_001035757.1:p.Ser15=
NM_001538.3:c.45C>T NP_001529.2:p.Ser15=
NM_001040667.3:c.45C>T NP_001035757.1:p.Ser15=
NM_001374674.1:c.45C>T NP_001361603.1:p.Ser15=
NM_001374675.1:c.45C>T MANE Select NP_001361604.1:p.Ser15=
NM_001538.4:c.45C>T NP_001529.2:p.Ser15=