Canonical Allele Identifier: CA8101774

Gene: HSF4

Linked Data

• dbSNP Id: rs371527905
• ExAC: 16:67199672 G / C
• gnomAD v2: 16-67199672-G-C
• gnomAD v3: 16-67165769-G-C
• gnomAD v4: 16-67165769-G-C
• MyVariant Identifiers: chr16:g.67199672G>C (hg19) ; chr16:g.67165769G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67165769G>C , CM000678.2:g.67165769G>C	GRCh38
NC_000016.9:g.67199672G>C , CM000678.1:g.67199672G>C	GRCh37
NC_000016.8:g.65757173G>C	NCBI36
NG_009294.1:g.7385G>C
NG_029566.1:g.268G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517867.2:n.566G>C
ENST00000523077.2:n.782G>C
ENST00000521374.6:c.283G>C MANE Select	ENSP00000430947.2:p.Glu95Gln
ENST00000434833.6:c.283G>C	ENSP00000403219.2:p.Glu95Gln
ENST00000517685.5:c.283G>C	ENSP00000428978.1:p.Glu95Gln
ENST00000517729.5:c.157G>C	ENSP00000430299.1:p.Glu53Gln
ENST00000518753.5:c.455G>C
ENST00000521314.5:c.*30G>C	ENSP00000429580.1:n.*30G>C
ENST00000521374.5:c.283G>C	ENSP00000430947.1:p.Glu95Gln
ENST00000521624.5:c.283G>C	ENSP00000428161.1:p.Glu95Gln
ENST00000522023.1:n.350G>C
ENST00000522295.5:c.283G>C	ENSP00000427832.1:p.Glu95Gln
ENST00000522870.5:n.502G>C
ENST00000523077.1:n.782G>C
ENST00000523562.5:c.283G>C	ENSP00000430631.1:p.Glu95Gln
ENST00000580114.5:c.1248G>C
ENST00000584272.5:c.283G>C	ENSP00000463706.1:p.Glu95Gln
NM_001040667.2:c.283G>C	NP_001035757.1:p.Glu95Gln
NM_001538.3:c.283G>C	NP_001529.2:p.Glu95Gln
NM_001040667.3:c.283G>C	NP_001035757.1:p.Glu95Gln
NM_001374674.1:c.283G>C	NP_001361603.1:p.Glu95Gln
NM_001374675.1:c.283G>C MANE Select	NP_001361604.1:p.Glu95Gln
NM_001538.4:c.283G>C	NP_001529.2:p.Glu95Gln