Canonical Allele Identifier: CA8101914

Gene: HSF4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67167110G>A , CM000678.2:g.67167110G>A	GRCh38
NC_000016.9:g.67201013G>A , CM000678.1:g.67201013G>A	GRCh37
NC_000016.8:g.65758514G>A	NCBI36
NG_009294.1:g.8726G>A
NG_029566.1:g.1609G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517867.2:n.910-10G>A
ENST00000523077.2:n.1126-10G>A
ENST00000683295.1:n.235-10G>A
ENST00000684701.1:n.351-10G>A
ENST00000521374.6:c.627-10G>A MANE Select	ENSP00000430947.2:n.627-10G>A
ENST00000434833.6:c.627-10G>A	ENSP00000403219.2:n.627-10G>A
ENST00000517680.5:n.247-10G>A
ENST00000517685.5:c.627-10G>A	ENSP00000428978.1:n.627-10G>A
ENST00000517729.5:c.438-10G>A	ENSP00000430299.1:n.438-10G>A
ENST00000517750.5:c.166-92G>A
ENST00000517867.1:n.129-10G>A
ENST00000519105.5:n.125-10G>A
ENST00000519224.5:c.216-10G>A
ENST00000521314.5:c.*374-10G>A	ENSP00000429580.1:n.*374-10G>A
ENST00000521374.5:c.627-10G>A	ENSP00000430947.1:n.627-10G>A
ENST00000521624.5:c.627-10G>A	ENSP00000428161.1:n.627-10G>A
ENST00000522027.5:n.205-10G>A
ENST00000522295.5:c.568-10G>A	ENSP00000427832.1:n.568-10G>A
ENST00000522459.5:n.186-10G>A
ENST00000522870.5:n.1095-10G>A
ENST00000523562.5:c.627-10G>A	ENSP00000430631.1:n.627-10G>A
ENST00000584272.5:c.627-10G>A	ENSP00000463706.1:n.627-10G>A
NM_001040667.2:c.627-10G>A	NP_001035757.1:n.627-10G>A
NM_001538.3:c.627-10G>A	NP_001529.2:n.627-10G>A
NM_001040667.3:c.627-10G>A	NP_001035757.1:n.627-10G>A
NM_001374674.1:c.627-10G>A	NP_001361603.1:n.627-10G>A
NM_001374675.1:c.627-10G>A MANE Select	NP_001361604.1:n.627-10G>A
NM_001538.4:c.627-10G>A	NP_001529.2:n.627-10G>A