Canonical Allele Identifier: CA2229202965

Gene: HSF4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67164788G= , CM000678.2:g.67164788G=	GRCh38
NC_000016.9:g.67198691G= , CM000678.1:g.67198691G=	GRCh37
NC_000016.8:g.65756192G=	NCBI36
NG_009294.1:g.6404G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521374.6:c.-24G= MANE Select	ENSP00000430947.2:n.-24G=
ENST00000434833.6:c.-24G=	ENSP00000403219.2:n.-24G=
ENST00000518227.1:c.619G=
ENST00000518753.5:c.295+644G=
ENST00000521314.5:c.-24G=	ENSP00000429580.1:n.-24G=
ENST00000522023.1:n.44G=
ENST00000522295.5:c.-24G=	ENSP00000427832.1:n.-24G=
ENST00000522870.5:n.108G=
ENST00000523360.1:n.468G=
ENST00000580114.5:c.942G=
NM_001040667.2:c.-24G=	NP_001035757.1:n.-24G=
NM_001538.3:c.-24G=	NP_001529.2:n.-24G=
NM_001040667.3:c.-24G=	NP_001035757.1:n.-24G=
NM_001374674.1:c.-24G=	NP_001361603.1:n.-24G=
NM_001374675.1:c.-24G= MANE Select	NP_001361604.1:n.-24G=
NM_001538.4:c.-24G=	NP_001529.2:n.-24G=