Canonical Allele Identifier: CA2842148519

Gene: HSF4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67164772G>A , CM000678.2:g.67164772G>A	GRCh38
NC_000016.9:g.67198675G>A , CM000678.1:g.67198675G>A	GRCh37
NC_000016.8:g.65756176G>A	NCBI36
NG_009294.1:g.6388G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521374.6:c.-40G>A MANE Select	ENSP00000430947.2:n.-40G>A
ENST00000434833.6:c.-40G>A	ENSP00000403219.2:n.-40G>A
ENST00000518227.1:c.603G>A
ENST00000518753.5:c.295+628G>A
ENST00000521314.5:c.-40G>A	ENSP00000429580.1:n.-40G>A
ENST00000522023.1:n.28G>A
ENST00000522295.5:c.-40G>A	ENSP00000427832.1:n.-40G>A
ENST00000522870.5:n.92G>A
ENST00000523360.1:n.452G>A
ENST00000580114.5:c.926G>A
NM_001040667.2:c.-40G>A	NP_001035757.1:n.-40G>A
NM_001538.3:c.-40G>A	NP_001529.2:n.-40G>A
NM_001040667.3:c.-40G>A	NP_001035757.1:n.-40G>A
NM_001374674.1:c.-40G>A	NP_001361603.1:n.-40G>A
NM_001374675.1:c.-40G>A MANE Select	NP_001361604.1:n.-40G>A
NM_001538.4:c.-40G>A	NP_001529.2:n.-40G>A