Canonical Allele Identifier: CA978396948

Gene: HSF4

Linked Data

• dbSNP Id: rs2031112398
• gnomAD v3: 16-67164759-TGACGAGCCCGCAGCG-T
• gnomAD v4: 16-67164759-TGACGAGCCCGCAGCG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67164761_67164775del , CM000678.2:g.67164761_67164775del	GRCh38
NC_000016.9:g.67198664_67198678del , CM000678.1:g.67198664_67198678del	GRCh37
NC_000016.8:g.65756165_65756179del	NCBI36
NG_009294.1:g.6377_6391del

Transcript Alleles

HGVS	Amino-acid change
ENST00000521374.6:c.-51_-37del MANE Select	ENSP00000430947.2:n.-51_-37del
ENST00000434833.6:c.-51_-37del	ENSP00000403219.2:n.-51_-37del
ENST00000518227.1:c.592_606del
ENST00000518753.5:c.295+617_295+631del
ENST00000522023.1:n.17_31del
ENST00000522295.5:c.-51_-37del	ENSP00000427832.1:n.-51_-37del
ENST00000522870.5:n.81_95del
ENST00000523360.1:n.441_455del
ENST00000580114.5:c.915_929del
NM_001040667.2:c.-51_-37del	NP_001035757.1:n.-51_-37del
NM_001538.3:c.-51_-37del	NP_001529.2:n.-51_-37del
NM_001040667.3:c.-51_-37del	NP_001035757.1:n.-51_-37del
NM_001374674.1:c.-51_-37del	NP_001361603.1:n.-51_-37del
NM_001374675.1:c.-51_-37del MANE Select	NP_001361604.1:n.-51_-37del
NM_001538.4:c.-51_-37del	NP_001529.2:n.-51_-37del