Canonical Allele Identifier: CA2633725007

Gene: HSF4

Linked Data

• gnomAD v4: 16-67164777-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67164777C>A , CM000678.2:g.67164777C>A	GRCh38
NC_000016.9:g.67198680C>A , CM000678.1:g.67198680C>A	GRCh37
NC_000016.8:g.65756181C>A	NCBI36
NG_009294.1:g.6393C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000521374.6:c.-35C>A MANE Select	ENSP00000430947.2:n.-35C>A
ENST00000434833.6:c.-35C>A	ENSP00000403219.2:n.-35C>A
ENST00000518227.1:c.608C>A
ENST00000518753.5:c.295+633C>A
ENST00000521314.5:c.-35C>A	ENSP00000429580.1:n.-35C>A
ENST00000522023.1:n.33C>A
ENST00000522295.5:c.-35C>A	ENSP00000427832.1:n.-35C>A
ENST00000522870.5:n.97C>A
ENST00000523360.1:n.457C>A
ENST00000580114.5:c.931C>A
NM_001040667.2:c.-35C>A	NP_001035757.1:n.-35C>A
NM_001538.3:c.-35C>A	NP_001529.2:n.-35C>A
NM_001040667.3:c.-35C>A	NP_001035757.1:n.-35C>A
NM_001374674.1:c.-35C>A	NP_001361603.1:n.-35C>A
NM_001374675.1:c.-35C>A MANE Select	NP_001361604.1:n.-35C>A
NM_001538.4:c.-35C>A	NP_001529.2:n.-35C>A