Canonical Allele Identifier: CA396263713

Gene: HSF4

Linked Data

• dbSNP Id: rs1216182543
• MyVariant Identifiers: chr16:g.67199651C>T (hg19) ; chr16:g.67165748C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67165748C>T , CM000678.2:g.67165748C>T	GRCh38
NC_000016.9:g.67199651C>T , CM000678.1:g.67199651C>T	GRCh37
NC_000016.8:g.65757152C>T	NCBI36
NG_009294.1:g.7364C>T
NG_029566.1:g.247C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517867.2:n.545C>T
ENST00000523077.2:n.761C>T
ENST00000521374.6:c.262C>T MANE Select	ENSP00000430947.2:p.Gln88Ter
ENST00000434833.6:c.262C>T	ENSP00000403219.2:p.Gln88Ter
ENST00000517685.5:c.262C>T	ENSP00000428978.1:p.Gln88Ter
ENST00000517729.5:c.136C>T	ENSP00000430299.1:p.Gln46Ter
ENST00000518753.5:c.434C>T
ENST00000521314.5:c.*9C>T	ENSP00000429580.1:n.*9C>T
ENST00000521374.5:c.262C>T	ENSP00000430947.1:p.Gln88Ter
ENST00000521624.5:c.262C>T	ENSP00000428161.1:p.Gln88Ter
ENST00000522023.1:n.329C>T
ENST00000522295.5:c.262C>T	ENSP00000427832.1:p.Gln88Ter
ENST00000522870.5:n.481C>T
ENST00000523077.1:n.761C>T
ENST00000523562.5:c.262C>T	ENSP00000430631.1:p.Gln88Ter
ENST00000580114.5:c.1227C>T
ENST00000584272.5:c.262C>T	ENSP00000463706.1:p.Gln88Ter
NM_001040667.2:c.262C>T	NP_001035757.1:p.Gln88Ter
NM_001538.3:c.262C>T	NP_001529.2:p.Gln88Ter
NM_001040667.3:c.262C>T	NP_001035757.1:p.Gln88Ter
NM_001374674.1:c.262C>T	NP_001361603.1:p.Gln88Ter
NM_001374675.1:c.262C>T MANE Select	NP_001361604.1:p.Gln88Ter
NM_001538.4:c.262C>T	NP_001529.2:p.Gln88Ter