Canonical Allele Identifier: CA2633725028

Gene: HSF4

Linked Data

• gnomAD v4: 16-67164796-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67164796G>T , CM000678.2:g.67164796G>T	GRCh38
NC_000016.9:g.67198699G>T , CM000678.1:g.67198699G>T	GRCh37
NC_000016.8:g.65756200G>T	NCBI36
NG_009294.1:g.6412G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521374.6:c.-16G>T MANE Select	ENSP00000430947.2:n.-16G>T
ENST00000434833.6:c.-16G>T	ENSP00000403219.2:n.-16G>T
ENST00000518227.1:c.627G>T
ENST00000518753.5:c.295+652G>T
ENST00000521314.5:c.-16G>T	ENSP00000429580.1:n.-16G>T
ENST00000521624.5:c.-16G>T	ENSP00000428161.1:n.-16G>T
ENST00000522023.1:n.52G>T
ENST00000522295.5:c.-16G>T	ENSP00000427832.1:n.-16G>T
ENST00000522870.5:n.116G>T
ENST00000523360.1:n.476G>T
ENST00000523562.5:c.-16G>T	ENSP00000430631.1:n.-16G>T
ENST00000580114.5:c.950G>T
NM_001040667.2:c.-16G>T	NP_001035757.1:n.-16G>T
NM_001538.3:c.-16G>T	NP_001529.2:n.-16G>T
NM_001040667.3:c.-16G>T	NP_001035757.1:n.-16G>T
NM_001374674.1:c.-16G>T	NP_001361603.1:n.-16G>T
NM_001374675.1:c.-16G>T MANE Select	NP_001361604.1:n.-16G>T
NM_001538.4:c.-16G>T	NP_001529.2:n.-16G>T