Canonical Allele Identifier: CA8102181

Gene: HSF4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67169647C>G , CM000678.2:g.67169647C>G	GRCh38
NC_000016.9:g.67203550C>G , CM000678.1:g.67203550C>G	GRCh37
NC_000016.8:g.65761051C>G	NCBI36
NG_009294.1:g.11263C>G
NG_029566.1:g.4146C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517867.2:n.1772C>G
ENST00000520528.2:c.641C>G
ENST00000523077.2:n.2018C>G
ENST00000682526.1:n.1167C>G
ENST00000684701.1:n.1243C>G
ENST00000521374.6:c.1341C>G MANE Select	ENSP00000430947.2:p.Leu447=
ENST00000434833.6:c.*289C>G	ENSP00000403219.2:n.*289C>G
ENST00000517685.5:c.1113C>G	ENSP00000428978.1:p.Leu371=
ENST00000519601.5:c.535C>G
ENST00000520304.5:c.352-81C>G
ENST00000520528.1:c.461C>G
ENST00000520833.5:n.1002C>G
ENST00000521314.5:c.*1088C>G	ENSP00000429580.1:n.*1088C>G
ENST00000521374.5:c.1341C>G	ENSP00000430947.1:p.Leu447=
ENST00000521624.5:c.*85C>G	ENSP00000428161.1:n.*85C>G
ENST00000521916.1:c.110C>G
ENST00000522295.5:c.*593C>G	ENSP00000427832.1:n.*593C>G
ENST00000523562.5:c.*571C>G	ENSP00000430631.1:n.*571C>G
ENST00000584272.5:c.1251C>G	ENSP00000463706.1:p.Leu417=
NM_001040667.2:c.1341C>G	NP_001035757.1:p.Leu447=
NM_001538.3:c.1251C>G	NP_001529.2:p.Leu417=
NM_001040667.3:c.1341C>G	NP_001035757.1:p.Leu447=
NM_001374674.1:c.1251C>G	NP_001361603.1:p.Leu417=
NM_001374675.1:c.1341C>G MANE Select	NP_001361604.1:p.Leu447=
NM_001538.4:c.1251C>G	NP_001529.2:p.Leu417=