Canonical Allele Identifier: CA396263358

Gene: HSF4

Linked Data

• MyVariant Identifiers: chr16:g.67199535T>A (hg19) ; chr16:g.67165632T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67165632T>A , CM000678.2:g.67165632T>A	GRCh38
NC_000016.9:g.67199535T>A , CM000678.1:g.67199535T>A	GRCh37
NC_000016.8:g.65757036T>A	NCBI36
NG_009294.1:g.7248T>A
NG_029566.1:g.131T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517867.2:n.515+2T>A
ENST00000523077.2:n.731+2T>A
ENST00000521374.6:c.232+2T>A MANE Select	ENSP00000430947.2:n.232+2T>A
ENST00000434833.6:c.232+2T>A	ENSP00000403219.2:n.232+2T>A
ENST00000517685.5:c.232+2T>A	ENSP00000428978.1:n.232+2T>A
ENST00000517729.5:c.106+2T>A	ENSP00000430299.1:n.106+2T>A
ENST00000518227.1:c.1463T>A
ENST00000518753.5:c.404+2T>A
ENST00000521314.5:c.124-87T>A	ENSP00000429580.1:n.124-87T>A
ENST00000521374.5:c.232+2T>A	ENSP00000430947.1:n.232+2T>A
ENST00000521624.5:c.232+2T>A	ENSP00000428161.1:n.232+2T>A
ENST00000522023.1:n.299+2T>A
ENST00000522295.5:c.232+2T>A	ENSP00000427832.1:n.232+2T>A
ENST00000522870.5:n.365T>A
ENST00000523077.1:n.731+2T>A
ENST00000523562.5:c.232+2T>A	ENSP00000430631.1:n.232+2T>A
ENST00000580114.5:c.1197+2T>A
ENST00000584272.5:c.232+2T>A	ENSP00000463706.1:n.232+2T>A
NM_001040667.2:c.232+2T>A	NP_001035757.1:n.232+2T>A
NM_001538.3:c.232+2T>A	NP_001529.2:n.232+2T>A
NM_001040667.3:c.232+2T>A	NP_001035757.1:n.232+2T>A
NM_001374674.1:c.232+2T>A	NP_001361603.1:n.232+2T>A
NM_001374675.1:c.232+2T>A MANE Select	NP_001361604.1:n.232+2T>A
NM_001538.4:c.232+2T>A	NP_001529.2:n.232+2T>A