Canonical Allele Identifier: CA396264658

Gene: HSF4

Linked Data

• MyVariant Identifiers: chr16:g.67199751T>A (hg19) ; chr16:g.67165848T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67165848T>A , CM000678.2:g.67165848T>A	GRCh38
NC_000016.9:g.67199751T>A , CM000678.1:g.67199751T>A	GRCh37
NC_000016.8:g.65757252T>A	NCBI36
NG_009294.1:g.7464T>A
NG_029566.1:g.347T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000517867.2:n.643+2T>A
ENST00000523077.2:n.859+2T>A
ENST00000521374.6:c.360+2T>A MANE Select	ENSP00000430947.2:n.360+2T>A
ENST00000434833.6:c.360+2T>A	ENSP00000403219.2:n.360+2T>A
ENST00000517685.5:c.360+2T>A	ENSP00000428978.1:n.360+2T>A
ENST00000517729.5:c.234+2T>A	ENSP00000430299.1:n.234+2T>A
ENST00000519224.5:c.8+2T>A
ENST00000521314.5:c.*107+2T>A	ENSP00000429580.1:n.*107+2T>A
ENST00000521374.5:c.360+2T>A	ENSP00000430947.1:n.360+2T>A
ENST00000521624.5:c.360+2T>A	ENSP00000428161.1:n.360+2T>A
ENST00000522023.1:n.427+2T>A
ENST00000522295.5:c.360+2T>A	ENSP00000427832.1:n.360+2T>A
ENST00000522870.5:n.579+2T>A
ENST00000523562.5:c.360+2T>A	ENSP00000430631.1:n.360+2T>A
ENST00000584272.5:c.360+2T>A	ENSP00000463706.1:n.360+2T>A
NM_001040667.2:c.360+2T>A	NP_001035757.1:n.360+2T>A
NM_001538.3:c.360+2T>A	NP_001529.2:n.360+2T>A
NM_001040667.3:c.360+2T>A	NP_001035757.1:n.360+2T>A
NM_001374674.1:c.360+2T>A	NP_001361603.1:n.360+2T>A
NM_001374675.1:c.360+2T>A MANE Select	NP_001361604.1:n.360+2T>A
NM_001538.4:c.360+2T>A	NP_001529.2:n.360+2T>A