Canonical Allele Identifier: CA2841487439

Gene: HSF4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67165939C>T , CM000678.2:g.67165939C>T	GRCh38
NC_000016.9:g.67199842C>T , CM000678.1:g.67199842C>T	GRCh37
NC_000016.8:g.65757343C>T	NCBI36
NG_009294.1:g.7555C>T
NG_029566.1:g.438C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517867.2:n.644-7C>T
ENST00000523077.2:n.860-7C>T
ENST00000521374.6:c.361-7C>T MANE Select	ENSP00000430947.2:n.361-7C>T
ENST00000434833.6:c.361-7C>T	ENSP00000403219.2:n.361-7C>T
ENST00000517685.5:c.361-7C>T	ENSP00000428978.1:n.361-7C>T
ENST00000517729.5:c.235-7C>T	ENSP00000430299.1:n.235-7C>T
ENST00000519224.5:c.9-7C>T
ENST00000521314.5:c.*108-7C>T	ENSP00000429580.1:n.*108-7C>T
ENST00000521374.5:c.361-7C>T	ENSP00000430947.1:n.361-7C>T
ENST00000521624.5:c.361-7C>T	ENSP00000428161.1:n.361-7C>T
ENST00000522023.1:n.428-7C>T
ENST00000522295.5:c.361-7C>T	ENSP00000427832.1:n.361-7C>T
ENST00000522870.5:n.580-7C>T
ENST00000523562.5:c.361-7C>T	ENSP00000430631.1:n.361-7C>T
ENST00000584272.5:c.361-7C>T	ENSP00000463706.1:n.361-7C>T
NM_001040667.2:c.361-7C>T	NP_001035757.1:n.361-7C>T
NM_001538.3:c.361-7C>T	NP_001529.2:n.361-7C>T
NM_001040667.3:c.361-7C>T	NP_001035757.1:n.361-7C>T
NM_001374674.1:c.361-7C>T	NP_001361603.1:n.361-7C>T
NM_001374675.1:c.361-7C>T MANE Select	NP_001361604.1:n.361-7C>T
NM_001538.4:c.361-7C>T	NP_001529.2:n.361-7C>T