Canonical Allele Identifier: CA8101661

Gene: HSF4

Linked Data

• dbSNP Id: rs749093208
• ExAC: 16:67198680 C / G
• gnomAD v2: 16-67198680-C-G
• gnomAD v3: 16-67164777-C-G
• gnomAD v4: 16-67164777-C-G
• MyVariant Identifiers: chr16:g.67198680C>G (hg19) ; chr16:g.67164777C>G (hg38)

Genomic Alleles

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

Transcript Alleles

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