Canonical Allele Identifier: CA396263087

Gene: HSF4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67165597A>G , CM000678.2:g.67165597A>G	GRCh38
NC_000016.9:g.67199500A>G , CM000678.1:g.67199500A>G	GRCh37
NC_000016.8:g.65757001A>G	NCBI36
NG_009294.1:g.7213A>G
NG_029566.1:g.96A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001374675.1:c.199A>G MANE Select	NP_001361604.1:p.Asn67Asp
ENST00000521374.6:c.199A>G MANE Select	ENSP00000430947.2:p.Asn67Asp
NM_001040667.2:c.199A>G	NP_001035757.1:p.Asn67Asp
NM_001040667.3:c.199A>G	NP_001035757.1:p.Asn67Asp
NM_001374674.1:c.199A>G	NP_001361603.1:p.Asn67Asp
NM_001538.3:c.199A>G	NP_001529.2:p.Asn67Asp
NM_001538.4:c.199A>G	NP_001529.2:p.Asn67Asp
ENST00000434833.6:c.199A>G	ENSP00000403219.2:p.Asn67Asp
ENST00000517685.5:c.199A>G	ENSP00000428978.1:p.Asn67Asp
ENST00000517729.5:c.73A>G	ENSP00000430299.1:p.Asn25Asp
ENST00000517867.2:n.482A>G
ENST00000518227.1:c.1428A>G
ENST00000518753.5:c.371A>G
ENST00000521314.5:c.124-122A>G	ENSP00000429580.1:n.124-122A>G
ENST00000521374.5:c.199A>G	ENSP00000430947.1:p.Asn67Asp
ENST00000521624.5:c.199A>G	ENSP00000428161.1:p.Asn67Asp
ENST00000522023.1:n.266A>G
ENST00000522295.5:c.199A>G	ENSP00000427832.1:p.Asn67Asp
ENST00000522870.5:n.330A>G
ENST00000523077.1:n.698A>G
ENST00000523077.2:n.698A>G
ENST00000523562.5:c.199A>G	ENSP00000430631.1:p.Asn67Asp
ENST00000580114.5:c.1164A>G
ENST00000584272.5:c.199A>G	ENSP00000463706.1:p.Asn67Asp