Canonical Allele Identifier: CA8101660

Gene: HSF4

Linked Data

• dbSNP Id: rs781324459
• ExAC: 16:67198672 G / T
• gnomAD v2: 16-67198672-G-T
• gnomAD v3: 16-67164769-G-T
• gnomAD v4: 16-67164769-G-T
• MyVariant Identifiers: chr16:g.67198672G>T (hg19) ; chr16:g.67164769G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67164769G>T , CM000678.2:g.67164769G>T	GRCh38
NC_000016.9:g.67198672G>T , CM000678.1:g.67198672G>T	GRCh37
NC_000016.8:g.65756173G>T	NCBI36
NG_009294.1:g.6385G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000521374.6:c.-43G>T MANE Select	ENSP00000430947.2:n.-43G>T
ENST00000434833.6:c.-43G>T	ENSP00000403219.2:n.-43G>T
ENST00000518227.1:c.600G>T
ENST00000518753.5:c.295+625G>T
ENST00000522023.1:n.25G>T
ENST00000522295.5:c.-43G>T	ENSP00000427832.1:n.-43G>T
ENST00000522870.5:n.89G>T
ENST00000523360.1:n.449G>T
ENST00000580114.5:c.923G>T
NM_001040667.2:c.-43G>T	NP_001035757.1:n.-43G>T
NM_001538.3:c.-43G>T	NP_001529.2:n.-43G>T
NM_001040667.3:c.-43G>T	NP_001035757.1:n.-43G>T
NM_001374674.1:c.-43G>T	NP_001361603.1:n.-43G>T
NM_001374675.1:c.-43G>T MANE Select	NP_001361604.1:n.-43G>T
NM_001538.4:c.-43G>T	NP_001529.2:n.-43G>T