Canonical Allele Identifier: CA10644082

Gene: HSF4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67169874G>T , CM000678.2:g.67169874G>T	GRCh38
NC_000016.9:g.67203777G>T , CM000678.1:g.67203777G>T	GRCh37
NC_000016.8:g.65761278G>T	NCBI36
NG_009294.1:g.11490G>T
NG_029566.1:g.4373G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001374675.1:c.*89G>T MANE Select	NP_001361604.1:n.*89G>T
ENST00000521374.6:c.*89G>T MANE Select	ENSP00000430947.2:n.*89G>T
NM_001040667.2:c.*89G>T	NP_001035757.1:n.*89G>T
NM_001040667.3:c.*89G>T	NP_001035757.1:n.*89G>T
NM_001374674.1:c.*89G>T	NP_001361603.1:n.*89G>T
NM_001538.3:c.*89G>T	NP_001529.2:n.*89G>T
NM_001538.4:c.*89G>T	NP_001529.2:n.*89G>T
ENST00000434833.6:c.*516G>T	ENSP00000403219.2:n.*516G>T
ENST00000520304.5:c.498G>T
ENST00000520528.1:c.688G>T
ENST00000520528.2:c.868G>T
ENST00000521314.5:c.*1315G>T	ENSP00000429580.1:n.*1315G>T
ENST00000521624.5:c.*312G>T	ENSP00000428161.1:n.*312G>T
ENST00000521916.1:c.337G>T
ENST00000522295.5:c.*820G>T	ENSP00000427832.1:n.*820G>T
ENST00000523077.2:n.2245G>T
ENST00000523562.5:c.*798G>T	ENSP00000430631.1:n.*798G>T
ENST00000584272.5:c.1478G>T	ENSP00000463706.1:n.1478G>T
ENST00000682526.1:n.1394G>T
ENST00000684701.1:n.1470G>T