Canonical Allele Identifier: CA396263947

Gene: HSF4

Linked Data

• dbSNP Id: rs1264444474
• gnomAD v2: 16-67199682-A-G
• gnomAD v4: 16-67165779-A-G
• MyVariant Identifiers: chr16:g.67199682A>G (hg19) ; chr16:g.67165779A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67165779A>G , CM000678.2:g.67165779A>G	GRCh38
NC_000016.9:g.67199682A>G , CM000678.1:g.67199682A>G	GRCh37
NC_000016.8:g.65757183A>G	NCBI36
NG_009294.1:g.7395A>G
NG_029566.1:g.278A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517867.2:n.576A>G
ENST00000523077.2:n.792A>G
ENST00000521374.6:c.293A>G MANE Select	ENSP00000430947.2:p.His98Arg
ENST00000434833.6:c.293A>G	ENSP00000403219.2:p.His98Arg
ENST00000517685.5:c.293A>G	ENSP00000428978.1:p.His98Arg
ENST00000517729.5:c.167A>G	ENSP00000430299.1:p.His56Arg
ENST00000518753.5:c.465A>G
ENST00000521314.5:c.*40A>G	ENSP00000429580.1:n.*40A>G
ENST00000521374.5:c.293A>G	ENSP00000430947.1:p.His98Arg
ENST00000521624.5:c.293A>G	ENSP00000428161.1:p.His98Arg
ENST00000522023.1:n.360A>G
ENST00000522295.5:c.293A>G	ENSP00000427832.1:p.His98Arg
ENST00000522870.5:n.512A>G
ENST00000523077.1:n.792A>G
ENST00000523562.5:c.293A>G	ENSP00000430631.1:p.His98Arg
ENST00000580114.5:c.1258A>G
ENST00000584272.5:c.293A>G	ENSP00000463706.1:p.His98Arg
NM_001040667.2:c.293A>G	NP_001035757.1:p.His98Arg
NM_001538.3:c.293A>G	NP_001529.2:p.His98Arg
NM_001040667.3:c.293A>G	NP_001035757.1:p.His98Arg
NM_001374674.1:c.293A>G	NP_001361603.1:p.His98Arg
NM_001374675.1:c.293A>G MANE Select	NP_001361604.1:p.His98Arg
NM_001538.4:c.293A>G	NP_001529.2:p.His98Arg