Canonical Allele Identifier: CA496072035

Gene: HSF4

Linked Data

• MyVariant Identifiers: chr16:g.67198750A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67164847A>C , CM000678.2:g.67164847A>C	GRCh38
NC_000016.9:g.67198750A>C , CM000678.1:g.67198750A>C	GRCh37
NC_000016.8:g.65756251A>C	NCBI36
NG_009294.1:g.6463A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521374.6:c.36A>C MANE Select	ENSP00000430947.2:p.Pro12=
ENST00000434833.6:c.36A>C	ENSP00000403219.2:p.Pro12=
ENST00000517685.5:c.36A>C	ENSP00000428978.1:p.Pro12=
ENST00000518227.1:c.678A>C
ENST00000518753.5:c.296-675A>C
ENST00000521314.5:c.36A>C	ENSP00000429580.1:p.Pro12=
ENST00000521374.5:c.36A>C	ENSP00000430947.1:p.Pro12=
ENST00000521624.5:c.36A>C	ENSP00000428161.1:p.Pro12=
ENST00000522023.1:n.103A>C
ENST00000522295.5:c.36A>C	ENSP00000427832.1:p.Pro12=
ENST00000522870.5:n.167A>C
ENST00000523562.5:c.36A>C	ENSP00000430631.1:p.Pro12=
ENST00000580114.5:c.1001A>C
ENST00000584272.5:c.36A>C	ENSP00000463706.1:p.Pro12=
NM_001040667.2:c.36A>C	NP_001035757.1:p.Pro12=
NM_001538.3:c.36A>C	NP_001529.2:p.Pro12=
NM_001040667.3:c.36A>C	NP_001035757.1:p.Pro12=
NM_001374674.1:c.36A>C	NP_001361603.1:p.Pro12=
NM_001374675.1:c.36A>C MANE Select	NP_001361604.1:p.Pro12=
NM_001538.4:c.36A>C	NP_001529.2:p.Pro12=