Canonical Allele Identifier: CA2633719576

Gene: HSF4

Linked Data

• gnomAD v4: 16-67165645-CCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67165646_67165647del , CM000678.2:g.67165646_67165647del	GRCh38
NC_000016.9:g.67199549_67199550del , CM000678.1:g.67199549_67199550del	GRCh37
NC_000016.8:g.65757050_65757051del	NCBI36
NG_009294.1:g.7262_7263del
NG_029566.1:g.145_146del

Transcript Alleles

HGVS	Amino-acid change
ENST00000517867.2:n.515+16_515+17del
ENST00000523077.2:n.731+16_731+17del
ENST00000521374.6:c.232+16_232+17del MANE Select	ENSP00000430947.2:n.232+16_232+17del
ENST00000434833.6:c.232+16_232+17del	ENSP00000403219.2:n.232+16_232+17del
ENST00000517685.5:c.232+16_232+17del	ENSP00000428978.1:n.232+16_232+17del
ENST00000517729.5:c.106+16_106+17del	ENSP00000430299.1:n.106+16_106+17del
ENST00000518753.5:c.404+16_404+17del
ENST00000521314.5:c.124-73_124-72del	ENSP00000429580.1:n.124-73_124-72del
ENST00000521374.5:c.232+16_232+17del	ENSP00000430947.1:n.232+16_232+17del
ENST00000521624.5:c.232+16_232+17del	ENSP00000428161.1:n.232+16_232+17del
ENST00000522023.1:n.299+16_299+17del
ENST00000522295.5:c.232+16_232+17del	ENSP00000427832.1:n.232+16_232+17del
ENST00000522870.5:n.379_380del
ENST00000523077.1:n.731+16_731+17del
ENST00000523562.5:c.232+16_232+17del	ENSP00000430631.1:n.232+16_232+17del
ENST00000580114.5:c.1197+16_1197+17del
ENST00000584272.5:c.232+16_232+17del	ENSP00000463706.1:n.232+16_232+17del
NM_001040667.2:c.232+16_232+17del	NP_001035757.1:n.232+16_232+17del
NM_001538.3:c.232+16_232+17del	NP_001529.2:n.232+16_232+17del
NM_001040667.3:c.232+16_232+17del	NP_001035757.1:n.232+16_232+17del
NM_001374674.1:c.232+16_232+17del	NP_001361603.1:n.232+16_232+17del
NM_001374675.1:c.232+16_232+17del MANE Select	NP_001361604.1:n.232+16_232+17del
NM_001538.4:c.232+16_232+17del	NP_001529.2:n.232+16_232+17del