Canonical Allele Identifier: CA2229202946

Gene: HSF4

Genomic Alleles

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

Transcript Alleles

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