Canonical Allele Identifier: CA396264554

Gene: HSF4

Linked Data

• ClinVar Variation Id: 459608
• ClinVar RCV Id: RCV000531113
• dbSNP Id: rs1555549881
• MyVariant Identifiers: chr16:g.67199739T>G (hg19) ; chr16:g.67165836T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67165836T>G , CM000678.2:g.67165836T>G	GRCh38
NC_000016.9:g.67199739T>G , CM000678.1:g.67199739T>G	GRCh37
NC_000016.8:g.65757240T>G	NCBI36
NG_009294.1:g.7452T>G
NG_029566.1:g.335T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517867.2:n.633T>G
ENST00000523077.2:n.849T>G
ENST00000521374.6:c.350T>G MANE Select	ENSP00000430947.2:p.Val117Gly
ENST00000434833.6:c.350T>G	ENSP00000403219.2:p.Val117Gly
ENST00000517685.5:c.350T>G	ENSP00000428978.1:p.Val117Gly
ENST00000517729.5:c.224T>G	ENSP00000430299.1:p.Val75Gly
ENST00000521314.5:c.*97T>G	ENSP00000429580.1:n.*97T>G
ENST00000521374.5:c.350T>G	ENSP00000430947.1:p.Val117Gly
ENST00000521624.5:c.350T>G	ENSP00000428161.1:p.Val117Gly
ENST00000522023.1:n.417T>G
ENST00000522295.5:c.350T>G	ENSP00000427832.1:p.Val117Gly
ENST00000522870.5:n.569T>G
ENST00000523562.5:c.350T>G	ENSP00000430631.1:p.Val117Gly
ENST00000584272.5:c.350T>G	ENSP00000463706.1:p.Val117Gly
NM_001040667.2:c.350T>G	NP_001035757.1:p.Val117Gly
NM_001538.3:c.350T>G	NP_001529.2:p.Val117Gly
NM_001040667.3:c.350T>G	NP_001035757.1:p.Val117Gly
NM_001374674.1:c.350T>G	NP_001361603.1:p.Val117Gly
NM_001374675.1:c.350T>G MANE Select	NP_001361604.1:p.Val117Gly
NM_001538.4:c.350T>G	NP_001529.2:p.Val117Gly