Canonical Allele Identifier: CA2229208789
Gene: HSF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67165637C= , CM000678.2:g.67165637C= GRCh38
NC_000016.9:g.67199540C= , CM000678.1:g.67199540C= GRCh37
NC_000016.8:g.65757041C= NCBI36
NG_009294.1:g.7253C=
NG_029566.1:g.136C=

Transcript Alleles

HGVS Amino-acid change
ENST00000517867.2:n.515+7C=
ENST00000523077.2:n.731+7C=
ENST00000521374.6:c.232+7C= MANE Select ENSP00000430947.2:n.232+7C=
ENST00000434833.6:c.232+7C= ENSP00000403219.2:n.232+7C=
ENST00000517685.5:c.232+7C= ENSP00000428978.1:n.232+7C=
ENST00000517729.5:c.106+7C= ENSP00000430299.1:n.106+7C=
ENST00000518227.1:c.1468C=
ENST00000518753.5:c.404+7C=
ENST00000521314.5:c.124-82C= ENSP00000429580.1:n.124-82C=
ENST00000521374.5:c.232+7C= ENSP00000430947.1:n.232+7C=
ENST00000521624.5:c.232+7C= ENSP00000428161.1:n.232+7C=
ENST00000522023.1:n.299+7C=
ENST00000522295.5:c.232+7C= ENSP00000427832.1:n.232+7C=
ENST00000522870.5:n.370C=
ENST00000523077.1:n.731+7C=
ENST00000523562.5:c.232+7C= ENSP00000430631.1:n.232+7C=
ENST00000580114.5:c.1197+7C=
ENST00000584272.5:c.232+7C= ENSP00000463706.1:n.232+7C=
NM_001040667.2:c.232+7C= NP_001035757.1:n.232+7C=
NM_001538.3:c.232+7C= NP_001529.2:n.232+7C=
NM_001040667.3:c.232+7C= NP_001035757.1:n.232+7C=
NM_001374674.1:c.232+7C= NP_001361603.1:n.232+7C=
NM_001374675.1:c.232+7C= MANE Select NP_001361604.1:n.232+7C=
NM_001538.4:c.232+7C= NP_001529.2:n.232+7C=