Canonical Allele Identifier: CA396263733

Gene: HSF4

Linked Data

• MyVariant Identifiers: chr16:g.67199654G>C (hg19) ; chr16:g.67165751G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67165751G>C , CM000678.2:g.67165751G>C	GRCh38
NC_000016.9:g.67199654G>C , CM000678.1:g.67199654G>C	GRCh37
NC_000016.8:g.65757155G>C	NCBI36
NG_009294.1:g.7367G>C
NG_029566.1:g.250G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000517867.2:n.548G>C
ENST00000523077.2:n.764G>C
ENST00000521374.6:c.265G>C MANE Select	ENSP00000430947.2:p.Gly89Arg
ENST00000434833.6:c.265G>C	ENSP00000403219.2:p.Gly89Arg
ENST00000517685.5:c.265G>C	ENSP00000428978.1:p.Gly89Arg
ENST00000517729.5:c.139G>C	ENSP00000430299.1:p.Gly47Arg
ENST00000518753.5:c.437G>C
ENST00000521314.5:c.*12G>C	ENSP00000429580.1:n.*12G>C
ENST00000521374.5:c.265G>C	ENSP00000430947.1:p.Gly89Arg
ENST00000521624.5:c.265G>C	ENSP00000428161.1:p.Gly89Arg
ENST00000522023.1:n.332G>C
ENST00000522295.5:c.265G>C	ENSP00000427832.1:p.Gly89Arg
ENST00000522870.5:n.484G>C
ENST00000523077.1:n.764G>C
ENST00000523562.5:c.265G>C	ENSP00000430631.1:p.Gly89Arg
ENST00000580114.5:c.1230G>C
ENST00000584272.5:c.265G>C	ENSP00000463706.1:p.Gly89Arg
NM_001040667.2:c.265G>C	NP_001035757.1:p.Gly89Arg
NM_001538.3:c.265G>C	NP_001529.2:p.Gly89Arg
NM_001040667.3:c.265G>C	NP_001035757.1:p.Gly89Arg
NM_001374674.1:c.265G>C	NP_001361603.1:p.Gly89Arg
NM_001374675.1:c.265G>C MANE Select	NP_001361604.1:p.Gly89Arg
NM_001538.4:c.265G>C	NP_001529.2:p.Gly89Arg