Canonical Allele Identifier: CA2229207920

Gene: HSF4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67164877C= , CM000678.2:g.67164877C=	GRCh38
NC_000016.9:g.67198780C= , CM000678.1:g.67198780C=	GRCh37
NC_000016.8:g.65756281C=	NCBI36
NG_009294.1:g.6493C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521374.6:c.66C= MANE Select	ENSP00000430947.2:p.Gly22=
ENST00000434833.6:c.66C=	ENSP00000403219.2:p.Gly22=
ENST00000517685.5:c.66C=	ENSP00000428978.1:p.Gly22=
ENST00000518227.1:c.708C=
ENST00000518753.5:c.296-645C=
ENST00000521314.5:c.66C=	ENSP00000429580.1:p.Gly22=
ENST00000521374.5:c.66C=	ENSP00000430947.1:p.Gly22=
ENST00000521624.5:c.66C=	ENSP00000428161.1:p.Gly22=
ENST00000522023.1:n.133C=
ENST00000522295.5:c.66C=	ENSP00000427832.1:p.Gly22=
ENST00000522870.5:n.197C=
ENST00000523562.5:c.66C=	ENSP00000430631.1:p.Gly22=
ENST00000580114.5:c.1031C=
ENST00000584272.5:c.66C=	ENSP00000463706.1:p.Gly22=
NM_001040667.2:c.66C=	NP_001035757.1:p.Gly22=
NM_001538.3:c.66C=	NP_001529.2:p.Gly22=
NM_001040667.3:c.66C=	NP_001035757.1:p.Gly22=
NM_001374674.1:c.66C=	NP_001361603.1:p.Gly22=
NM_001374675.1:c.66C= MANE Select	NP_001361604.1:p.Gly22=
NM_001538.4:c.66C=	NP_001529.2:p.Gly22=