Canonical Allele Identifier: CA10644081

Gene: HSF4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67167940C>A , CM000678.2:g.67167940C>A	GRCh38
NC_000016.9:g.67201843C>A , CM000678.1:g.67201843C>A	GRCh37
NC_000016.8:g.65759344C>A	NCBI36
NG_009294.1:g.9556C>A
NG_029566.1:g.2439C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001374675.1:c.1075C>A MANE Select	NP_001361604.1:p.Pro359Thr
ENST00000521374.6:c.1075C>A MANE Select	ENSP00000430947.2:p.Pro359Thr
NM_001040667.2:c.1075C>A	NP_001035757.1:p.Pro359Thr
NM_001040667.3:c.1075C>A	NP_001035757.1:p.Pro359Thr
NM_001374674.1:c.985C>A	NP_001361603.1:p.Pro329Thr
NM_001538.3:c.985C>A	NP_001529.2:p.Pro329Thr
NM_001538.4:c.985C>A	NP_001529.2:p.Pro329Thr
ENST00000434833.6:c.*23C>A	ENSP00000403219.2:n.*23C>A
ENST00000517685.5:c.854+341C>A	ENSP00000428978.1:n.854+341C>A
ENST00000517750.5:c.428C>A
ENST00000517867.2:n.1506C>A
ENST00000519601.5:c.269C>A
ENST00000520304.5:c.102C>A
ENST00000520528.1:c.265C>A
ENST00000520528.2:c.445C>A
ENST00000520833.5:n.277C>A
ENST00000521314.5:c.*822C>A	ENSP00000429580.1:n.*822C>A
ENST00000521374.5:c.1075C>A	ENSP00000430947.1:p.Pro359Thr
ENST00000521624.5:c.846C>A	ENSP00000428161.1:p.Tyr282Ter
ENST00000522295.5:c.*327C>A	ENSP00000427832.1:n.*327C>A
ENST00000522870.5:n.1539C>A
ENST00000523077.2:n.1470C>A
ENST00000523562.5:c.*23C>A	ENSP00000430631.1:n.*23C>A
ENST00000584272.5:c.985C>A	ENSP00000463706.1:p.Pro329Thr
ENST00000682677.1:n.280C>A
ENST00000683295.1:n.683C>A
ENST00000684701.1:n.695C>A