Canonical Allele Identifier: CA396264396

Gene: HSF4

Linked Data

• MyVariant Identifiers: chr16:g.67199724A>C (hg19) ; chr16:g.67165821A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67165821A>C , CM000678.2:g.67165821A>C	GRCh38
NC_000016.9:g.67199724A>C , CM000678.1:g.67199724A>C	GRCh37
NC_000016.8:g.65757225A>C	NCBI36
NG_009294.1:g.7437A>C
NG_029566.1:g.320A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517867.2:n.618A>C
ENST00000523077.2:n.834A>C
ENST00000521374.6:c.335A>C MANE Select	ENSP00000430947.2:p.Gln112Pro
ENST00000434833.6:c.335A>C	ENSP00000403219.2:p.Gln112Pro
ENST00000517685.5:c.335A>C	ENSP00000428978.1:p.Gln112Pro
ENST00000517729.5:c.209A>C	ENSP00000430299.1:p.Gln70Pro
ENST00000521314.5:c.*82A>C	ENSP00000429580.1:n.*82A>C
ENST00000521374.5:c.335A>C	ENSP00000430947.1:p.Gln112Pro
ENST00000521624.5:c.335A>C	ENSP00000428161.1:p.Gln112Pro
ENST00000522023.1:n.402A>C
ENST00000522295.5:c.335A>C	ENSP00000427832.1:p.Gln112Pro
ENST00000522870.5:n.554A>C
ENST00000523562.5:c.335A>C	ENSP00000430631.1:p.Gln112Pro
ENST00000584272.5:c.335A>C	ENSP00000463706.1:p.Gln112Pro
NM_001040667.2:c.335A>C	NP_001035757.1:p.Gln112Pro
NM_001538.3:c.335A>C	NP_001529.2:p.Gln112Pro
NM_001040667.3:c.335A>C	NP_001035757.1:p.Gln112Pro
NM_001374674.1:c.335A>C	NP_001361603.1:p.Gln112Pro
NM_001374675.1:c.335A>C MANE Select	NP_001361604.1:p.Gln112Pro
NM_001538.4:c.335A>C	NP_001529.2:p.Gln112Pro