Canonical Allele Identifier: CA396264213

Gene: HSF4

Linked Data

• MyVariant Identifiers: chr16:g.67199708G>A (hg19) ; chr16:g.67165805G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67165805G>A , CM000678.2:g.67165805G>A	GRCh38
NC_000016.9:g.67199708G>A , CM000678.1:g.67199708G>A	GRCh37
NC_000016.8:g.65757209G>A	NCBI36
NG_009294.1:g.7421G>A
NG_029566.1:g.304G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517867.2:n.602G>A
ENST00000523077.2:n.818G>A
ENST00000521374.6:c.319G>A MANE Select	ENSP00000430947.2:p.Val107Met
ENST00000434833.6:c.319G>A	ENSP00000403219.2:p.Val107Met
ENST00000517685.5:c.319G>A	ENSP00000428978.1:p.Val107Met
ENST00000517729.5:c.193G>A	ENSP00000430299.1:p.Val65Met
ENST00000518753.5:c.491G>A
ENST00000521314.5:c.*66G>A	ENSP00000429580.1:n.*66G>A
ENST00000521374.5:c.319G>A	ENSP00000430947.1:p.Val107Met
ENST00000521624.5:c.319G>A	ENSP00000428161.1:p.Val107Met
ENST00000522023.1:n.386G>A
ENST00000522295.5:c.319G>A	ENSP00000427832.1:p.Val107Met
ENST00000522870.5:n.538G>A
ENST00000523077.1:n.818G>A
ENST00000523562.5:c.319G>A	ENSP00000430631.1:p.Val107Met
ENST00000580114.5:c.1284G>A
ENST00000584272.5:c.319G>A	ENSP00000463706.1:p.Val107Met
NM_001040667.2:c.319G>A	NP_001035757.1:p.Val107Met
NM_001538.3:c.319G>A	NP_001529.2:p.Val107Met
NM_001040667.3:c.319G>A	NP_001035757.1:p.Val107Met
NM_001374674.1:c.319G>A	NP_001361603.1:p.Val107Met
NM_001374675.1:c.319G>A MANE Select	NP_001361604.1:p.Val107Met
NM_001538.4:c.319G>A	NP_001529.2:p.Val107Met