Canonical Allele Identifier: CA2633725715
Gene: HSF4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67165951dup , CM000678.2:g.67165951dup GRCh38
NC_000016.9:g.67199854dup , CM000678.1:g.67199854dup GRCh37
NC_000016.8:g.65757355dup NCBI36
NG_009294.1:g.7567dup
NG_029566.1:g.450dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000517867.2:n.649dup
ENST00000523077.2:n.865dup
ENST00000521374.6:c.366dup MANE Select ENSP00000430947.2:p.Ala123ArgfsTer?
ENST00000434833.6:c.366dup ENSP00000403219.2:p.Ala123ArgfsTer?
ENST00000517685.5:c.366dup ENSP00000428978.1:p.Ala123ArgfsTer?
ENST00000517729.5:c.240dup ENSP00000430299.1:p.Ala81ArgfsTer?
ENST00000519224.5:c.14dup
ENST00000521314.5:c.*113dup ENSP00000429580.1:n.*113dup
ENST00000521374.5:c.366dup ENSP00000430947.1:p.Ala123ArgfsTer?
ENST00000521624.5:c.366dup ENSP00000428161.1:p.Ala123ArgfsTer?
ENST00000522023.1:n.433dup
ENST00000522295.5:c.366dup ENSP00000427832.1:p.Ala123ArgfsTer?
ENST00000522870.5:n.585dup
ENST00000523562.5:c.366dup ENSP00000430631.1:p.Ala123ArgfsTer?
ENST00000584272.5:c.366dup ENSP00000463706.1:p.Ala123ArgfsTer?
NM_001040667.2:c.366dup NP_001035757.1:p.Ala123ArgfsTer?
NM_001538.3:c.366dup NP_001529.2:p.Ala123ArgfsTer?
NM_001040667.3:c.366dup NP_001035757.1:p.Ala123ArgfsTer?
NM_001374674.1:c.366dup NP_001361603.1:p.Ala123ArgfsTer?
NM_001374675.1:c.366dup MANE Select NP_001361604.1:p.Ala123ArgfsTer?
NM_001538.4:c.366dup NP_001529.2:p.Ala123ArgfsTer?