Canonical Allele Identifier: CA2633719578

Gene: HSF4

Linked Data

• gnomAD v4: 16-67165646-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67165646C>A , CM000678.2:g.67165646C>A	GRCh38
NC_000016.9:g.67199549C>A , CM000678.1:g.67199549C>A	GRCh37
NC_000016.8:g.65757050C>A	NCBI36
NG_009294.1:g.7262C>A
NG_029566.1:g.145C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517867.2:n.515+16C>A
ENST00000523077.2:n.731+16C>A
ENST00000521374.6:c.232+16C>A MANE Select	ENSP00000430947.2:n.232+16C>A
ENST00000434833.6:c.232+16C>A	ENSP00000403219.2:n.232+16C>A
ENST00000517685.5:c.232+16C>A	ENSP00000428978.1:n.232+16C>A
ENST00000517729.5:c.106+16C>A	ENSP00000430299.1:n.106+16C>A
ENST00000518753.5:c.404+16C>A
ENST00000521314.5:c.124-73C>A	ENSP00000429580.1:n.124-73C>A
ENST00000521374.5:c.232+16C>A	ENSP00000430947.1:n.232+16C>A
ENST00000521624.5:c.232+16C>A	ENSP00000428161.1:n.232+16C>A
ENST00000522023.1:n.299+16C>A
ENST00000522295.5:c.232+16C>A	ENSP00000427832.1:n.232+16C>A
ENST00000522870.5:n.379C>A
ENST00000523077.1:n.731+16C>A
ENST00000523562.5:c.232+16C>A	ENSP00000430631.1:n.232+16C>A
ENST00000580114.5:c.1197+16C>A
ENST00000584272.5:c.232+16C>A	ENSP00000463706.1:n.232+16C>A
NM_001040667.2:c.232+16C>A	NP_001035757.1:n.232+16C>A
NM_001538.3:c.232+16C>A	NP_001529.2:n.232+16C>A
NM_001040667.3:c.232+16C>A	NP_001035757.1:n.232+16C>A
NM_001374674.1:c.232+16C>A	NP_001361603.1:n.232+16C>A
NM_001374675.1:c.232+16C>A MANE Select	NP_001361604.1:n.232+16C>A
NM_001538.4:c.232+16C>A	NP_001529.2:n.232+16C>A