Canonical Allele Identifier: CA396269335

Gene: HSF4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67167129G>C , CM000678.2:g.67167129G>C	GRCh38
NC_000016.9:g.67201032G>C , CM000678.1:g.67201032G>C	GRCh37
NC_000016.8:g.65758533G>C	NCBI36
NG_009294.1:g.8745G>C
NG_029566.1:g.1628G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001374675.1:c.636G>C MANE Select	NP_001361604.1:p.Met212Ile
ENST00000521374.6:c.636G>C MANE Select	ENSP00000430947.2:p.Met212Ile
NM_001040667.2:c.636G>C	NP_001035757.1:p.Met212Ile
NM_001040667.3:c.636G>C	NP_001035757.1:p.Met212Ile
NM_001374674.1:c.636G>C	NP_001361603.1:p.Met212Ile
NM_001538.3:c.636G>C	NP_001529.2:p.Met212Ile
NM_001538.4:c.636G>C	NP_001529.2:p.Met212Ile
ENST00000434833.6:c.636G>C	ENSP00000403219.2:p.Met212Ile
ENST00000517680.5:n.256G>C
ENST00000517685.5:c.636G>C	ENSP00000428978.1:p.Met212Ile
ENST00000517729.5:c.447G>C	ENSP00000430299.1:p.Met149Ile
ENST00000517750.5:c.166-73G>C
ENST00000517867.1:n.138G>C
ENST00000517867.2:n.919G>C
ENST00000519105.5:n.134G>C
ENST00000519224.5:c.225G>C
ENST00000520528.2:c.10G>C
ENST00000521314.5:c.*383G>C	ENSP00000429580.1:n.*383G>C
ENST00000521374.5:c.636G>C	ENSP00000430947.1:p.Met212Ile
ENST00000521624.5:c.636G>C	ENSP00000428161.1:p.Met212Ile
ENST00000522027.5:n.214G>C
ENST00000522295.5:c.577G>C	ENSP00000427832.1:p.Ala193Pro
ENST00000522459.5:n.195G>C
ENST00000522870.5:n.1104G>C
ENST00000523077.2:n.1135G>C
ENST00000523562.5:c.636G>C	ENSP00000430631.1:p.Met212Ile
ENST00000584272.5:c.636G>C	ENSP00000463706.1:p.Met212Ile
ENST00000683295.1:n.244G>C
ENST00000684701.1:n.360G>C