Canonical Allele Identifier: CA496072212

Gene: HSF4

Linked Data

• gnomAD v4: 16-67165837-G-T
• MyVariant Identifiers: chr16:g.67199740G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67165837G>T , CM000678.2:g.67165837G>T	GRCh38
NC_000016.9:g.67199740G>T , CM000678.1:g.67199740G>T	GRCh37
NC_000016.8:g.65757241G>T	NCBI36
NG_009294.1:g.7453G>T
NG_029566.1:g.336G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000517867.2:n.634G>T
ENST00000523077.2:n.850G>T
ENST00000521374.6:c.351G>T MANE Select	ENSP00000430947.2:p.Val117=
ENST00000434833.6:c.351G>T	ENSP00000403219.2:p.Val117=
ENST00000517685.5:c.351G>T	ENSP00000428978.1:p.Val117=
ENST00000517729.5:c.225G>T	ENSP00000430299.1:p.Val75=
ENST00000521314.5:c.*98G>T	ENSP00000429580.1:n.*98G>T
ENST00000521374.5:c.351G>T	ENSP00000430947.1:p.Val117=
ENST00000521624.5:c.351G>T	ENSP00000428161.1:p.Val117=
ENST00000522023.1:n.418G>T
ENST00000522295.5:c.351G>T	ENSP00000427832.1:p.Val117=
ENST00000522870.5:n.570G>T
ENST00000523562.5:c.351G>T	ENSP00000430631.1:p.Val117=
ENST00000584272.5:c.351G>T	ENSP00000463706.1:p.Val117=
NM_001040667.2:c.351G>T	NP_001035757.1:p.Val117=
NM_001538.3:c.351G>T	NP_001529.2:p.Val117=
NM_001040667.3:c.351G>T	NP_001035757.1:p.Val117=
NM_001374674.1:c.351G>T	NP_001361603.1:p.Val117=
NM_001374675.1:c.351G>T MANE Select	NP_001361604.1:p.Val117=
NM_001538.4:c.351G>T	NP_001529.2:p.Val117=