Canonical Allele Identifier: CA496072041

Gene: HSF4

Linked Data

• MyVariant Identifiers: chr16:g.67198756C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67164853C>A , CM000678.2:g.67164853C>A	GRCh38
NC_000016.9:g.67198756C>A , CM000678.1:g.67198756C>A	GRCh37
NC_000016.8:g.65756257C>A	NCBI36
NG_009294.1:g.6469C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521374.6:c.42C>A MANE Select	ENSP00000430947.2:p.Pro14=
ENST00000434833.6:c.42C>A	ENSP00000403219.2:p.Pro14=
ENST00000517685.5:c.42C>A	ENSP00000428978.1:p.Pro14=
ENST00000518227.1:c.684C>A
ENST00000518753.5:c.296-669C>A
ENST00000521314.5:c.42C>A	ENSP00000429580.1:p.Pro14=
ENST00000521374.5:c.42C>A	ENSP00000430947.1:p.Pro14=
ENST00000521624.5:c.42C>A	ENSP00000428161.1:p.Pro14=
ENST00000522023.1:n.109C>A
ENST00000522295.5:c.42C>A	ENSP00000427832.1:p.Pro14=
ENST00000522870.5:n.173C>A
ENST00000523562.5:c.42C>A	ENSP00000430631.1:p.Pro14=
ENST00000580114.5:c.1007C>A
ENST00000584272.5:c.42C>A	ENSP00000463706.1:p.Pro14=
NM_001040667.2:c.42C>A	NP_001035757.1:p.Pro14=
NM_001538.3:c.42C>A	NP_001529.2:p.Pro14=
NM_001040667.3:c.42C>A	NP_001035757.1:p.Pro14=
NM_001374674.1:c.42C>A	NP_001361603.1:p.Pro14=
NM_001374675.1:c.42C>A MANE Select	NP_001361604.1:p.Pro14=
NM_001538.4:c.42C>A	NP_001529.2:p.Pro14=