Canonical Allele Identifier: CA2576024675

Gene: HSF4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67164771A>C , CM000678.2:g.67164771A>C	GRCh38
NC_000016.9:g.67198674A>C , CM000678.1:g.67198674A>C	GRCh37
NC_000016.8:g.65756175A>C	NCBI36
NG_009294.1:g.6387A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000521374.6:c.-41A>C MANE Select	ENSP00000430947.2:n.-41A>C
ENST00000434833.6:c.-41A>C	ENSP00000403219.2:n.-41A>C
ENST00000518227.1:c.602A>C
ENST00000518753.5:c.295+627A>C
ENST00000521314.5:c.-41A>C	ENSP00000429580.1:n.-41A>C
ENST00000522023.1:n.27A>C
ENST00000522295.5:c.-41A>C	ENSP00000427832.1:n.-41A>C
ENST00000522870.5:n.91A>C
ENST00000523360.1:n.451A>C
ENST00000580114.5:c.925A>C
NM_001040667.2:c.-41A>C	NP_001035757.1:n.-41A>C
NM_001538.3:c.-41A>C	NP_001529.2:n.-41A>C
NM_001040667.3:c.-41A>C	NP_001035757.1:n.-41A>C
NM_001374674.1:c.-41A>C	NP_001361603.1:n.-41A>C
NM_001374675.1:c.-41A>C MANE Select	NP_001361604.1:n.-41A>C
NM_001538.4:c.-41A>C	NP_001529.2:n.-41A>C