Canonical Allele Identifier: CA282288500

Gene: HSF4

Linked Data

• dbSNP Id: rs936116065
• gnomAD v3: 16-67164770-C-G
• gnomAD v4: 16-67164770-C-G
• MyVariant Identifiers: chr16:g.67198673C>G (hg19) ; chr16:g.67164770C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67164770C>G , CM000678.2:g.67164770C>G	GRCh38
NC_000016.9:g.67198673C>G , CM000678.1:g.67198673C>G	GRCh37
NC_000016.8:g.65756174C>G	NCBI36
NG_009294.1:g.6386C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000521374.6:c.-42C>G MANE Select	ENSP00000430947.2:n.-42C>G
ENST00000434833.6:c.-42C>G	ENSP00000403219.2:n.-42C>G
ENST00000518227.1:c.601C>G
ENST00000518753.5:c.295+626C>G
ENST00000522023.1:n.26C>G
ENST00000522295.5:c.-42C>G	ENSP00000427832.1:n.-42C>G
ENST00000522870.5:n.90C>G
ENST00000523360.1:n.450C>G
ENST00000580114.5:c.924C>G
NM_001040667.2:c.-42C>G	NP_001035757.1:n.-42C>G
NM_001538.3:c.-42C>G	NP_001529.2:n.-42C>G
NM_001040667.3:c.-42C>G	NP_001035757.1:n.-42C>G
NM_001374674.1:c.-42C>G	NP_001361603.1:n.-42C>G
NM_001374675.1:c.-42C>G MANE Select	NP_001361604.1:n.-42C>G
NM_001538.4:c.-42C>G	NP_001529.2:n.-42C>G