Canonical Allele Identifier: CA8101665

Gene: HSF4

Linked Data

• dbSNP Id: rs772020199
• ExAC: 16:67198686 C / G
• gnomAD v2: 16-67198686-C-G
• gnomAD v4: 16-67164783-C-G
• MyVariant Identifiers: chr16:g.67198686C>G (hg19) ; chr16:g.67164783C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67164783C>G , CM000678.2:g.67164783C>G	GRCh38
NC_000016.9:g.67198686C>G , CM000678.1:g.67198686C>G	GRCh37
NC_000016.8:g.65756187C>G	NCBI36
NG_009294.1:g.6399C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521374.6:c.-29C>G MANE Select	ENSP00000430947.2:n.-29C>G
ENST00000434833.6:c.-29C>G	ENSP00000403219.2:n.-29C>G
ENST00000518227.1:c.614C>G
ENST00000518753.5:c.295+639C>G
ENST00000521314.5:c.-29C>G	ENSP00000429580.1:n.-29C>G
ENST00000522023.1:n.39C>G
ENST00000522295.5:c.-29C>G	ENSP00000427832.1:n.-29C>G
ENST00000522870.5:n.103C>G
ENST00000523360.1:n.463C>G
ENST00000580114.5:c.937C>G
NM_001040667.2:c.-29C>G	NP_001035757.1:n.-29C>G
NM_001538.3:c.-29C>G	NP_001529.2:n.-29C>G
NM_001040667.3:c.-29C>G	NP_001035757.1:n.-29C>G
NM_001374674.1:c.-29C>G	NP_001361603.1:n.-29C>G
NM_001374675.1:c.-29C>G MANE Select	NP_001361604.1:n.-29C>G
NM_001538.4:c.-29C>G	NP_001529.2:n.-29C>G