Canonical Allele Identifier: CA2229209026
Gene: HSF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67165847G= , CM000678.2:g.67165847G= GRCh38
NC_000016.9:g.67199750G= , CM000678.1:g.67199750G= GRCh37
NC_000016.8:g.65757251G= NCBI36
NG_009294.1:g.7463G=
NG_029566.1:g.346G=

Transcript Alleles

HGVS Amino-acid change
ENST00000517867.2:n.643+1G=
ENST00000523077.2:n.859+1G=
ENST00000521374.6:c.360+1G= MANE Select ENSP00000430947.2:n.360+1G=
ENST00000434833.6:c.360+1G= ENSP00000403219.2:n.360+1G=
ENST00000517685.5:c.360+1G= ENSP00000428978.1:n.360+1G=
ENST00000517729.5:c.234+1G= ENSP00000430299.1:n.234+1G=
ENST00000519224.5:c.8+1G=
ENST00000521314.5:c.*107+1G= ENSP00000429580.1:n.*107+1G=
ENST00000521374.5:c.360+1G= ENSP00000430947.1:n.360+1G=
ENST00000521624.5:c.360+1G= ENSP00000428161.1:n.360+1G=
ENST00000522023.1:n.427+1G=
ENST00000522295.5:c.360+1G= ENSP00000427832.1:n.360+1G=
ENST00000522870.5:n.579+1G=
ENST00000523562.5:c.360+1G= ENSP00000430631.1:n.360+1G=
ENST00000584272.5:c.360+1G= ENSP00000463706.1:n.360+1G=
NM_001040667.2:c.360+1G= NP_001035757.1:n.360+1G=
NM_001538.3:c.360+1G= NP_001529.2:n.360+1G=
NM_001040667.3:c.360+1G= NP_001035757.1:n.360+1G=
NM_001374674.1:c.360+1G= NP_001361603.1:n.360+1G=
NM_001374675.1:c.360+1G= MANE Select NP_001361604.1:n.360+1G=
NM_001538.4:c.360+1G= NP_001529.2:n.360+1G=