Canonical Allele Identifier: CA496072125

Gene: HSF4

Linked Data

• MyVariant Identifiers: chr16:g.67199668G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67165765G>A , CM000678.2:g.67165765G>A	GRCh38
NC_000016.9:g.67199668G>A , CM000678.1:g.67199668G>A	GRCh37
NC_000016.8:g.65757169G>A	NCBI36
NG_009294.1:g.7381G>A
NG_029566.1:g.264G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517867.2:n.562G>A
ENST00000523077.2:n.778G>A
ENST00000521374.6:c.279G>A MANE Select	ENSP00000430947.2:p.Arg93=
ENST00000434833.6:c.279G>A	ENSP00000403219.2:p.Arg93=
ENST00000517685.5:c.279G>A	ENSP00000428978.1:p.Arg93=
ENST00000517729.5:c.153G>A	ENSP00000430299.1:p.Arg51=
ENST00000518753.5:c.451G>A
ENST00000521314.5:c.*26G>A	ENSP00000429580.1:n.*26G>A
ENST00000521374.5:c.279G>A	ENSP00000430947.1:p.Arg93=
ENST00000521624.5:c.279G>A	ENSP00000428161.1:p.Arg93=
ENST00000522023.1:n.346G>A
ENST00000522295.5:c.279G>A	ENSP00000427832.1:p.Arg93=
ENST00000522870.5:n.498G>A
ENST00000523077.1:n.778G>A
ENST00000523562.5:c.279G>A	ENSP00000430631.1:p.Arg93=
ENST00000580114.5:c.1244G>A
ENST00000584272.5:c.279G>A	ENSP00000463706.1:p.Arg93=
NM_001040667.2:c.279G>A	NP_001035757.1:p.Arg93=
NM_001538.3:c.279G>A	NP_001529.2:p.Arg93=
NM_001040667.3:c.279G>A	NP_001035757.1:p.Arg93=
NM_001374674.1:c.279G>A	NP_001361603.1:p.Arg93=
NM_001374675.1:c.279G>A MANE Select	NP_001361604.1:p.Arg93=
NM_001538.4:c.279G>A	NP_001529.2:p.Arg93=