Canonical Allele Identifier: CA623117443

Gene: HSF4

Linked Data

• dbSNP Id: rs112061587
• gnomAD v2: 16-67199545-C-T
• gnomAD v4: 16-67165642-C-T
• MyVariant Identifiers: chr16:g.67199545C>T (hg19) ; chr16:g.67165642C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67165642C>T , CM000678.2:g.67165642C>T	GRCh38
NC_000016.9:g.67199545C>T , CM000678.1:g.67199545C>T	GRCh37
NC_000016.8:g.65757046C>T	NCBI36
NG_009294.1:g.7258C>T
NG_029566.1:g.141C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000517867.2:n.515+12C>T
ENST00000523077.2:n.731+12C>T
ENST00000521374.6:c.232+12C>T MANE Select	ENSP00000430947.2:n.232+12C>T
ENST00000434833.6:c.232+12C>T	ENSP00000403219.2:n.232+12C>T
ENST00000517685.5:c.232+12C>T	ENSP00000428978.1:n.232+12C>T
ENST00000517729.5:c.106+12C>T	ENSP00000430299.1:n.106+12C>T
ENST00000518227.1:c.1473C>T
ENST00000518753.5:c.404+12C>T
ENST00000521314.5:c.124-77C>T	ENSP00000429580.1:n.124-77C>T
ENST00000521374.5:c.232+12C>T	ENSP00000430947.1:n.232+12C>T
ENST00000521624.5:c.232+12C>T	ENSP00000428161.1:n.232+12C>T
ENST00000522023.1:n.299+12C>T
ENST00000522295.5:c.232+12C>T	ENSP00000427832.1:n.232+12C>T
ENST00000522870.5:n.375C>T
ENST00000523077.1:n.731+12C>T
ENST00000523562.5:c.232+12C>T	ENSP00000430631.1:n.232+12C>T
ENST00000580114.5:c.1197+12C>T
ENST00000584272.5:c.232+12C>T	ENSP00000463706.1:n.232+12C>T
NM_001040667.2:c.232+12C>T	NP_001035757.1:n.232+12C>T
NM_001538.3:c.232+12C>T	NP_001529.2:n.232+12C>T
NM_001040667.3:c.232+12C>T	NP_001035757.1:n.232+12C>T
NM_001374674.1:c.232+12C>T	NP_001361603.1:n.232+12C>T
NM_001374675.1:c.232+12C>T MANE Select	NP_001361604.1:n.232+12C>T
NM_001538.4:c.232+12C>T	NP_001529.2:n.232+12C>T