Canonical Allele Identifier: CA396263348

Gene: HSF4

Linked Data

• MyVariant Identifiers: chr16:g.67199534G>C (hg19) ; chr16:g.67165631G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67165631G>C , CM000678.2:g.67165631G>C	GRCh38
NC_000016.9:g.67199534G>C , CM000678.1:g.67199534G>C	GRCh37
NC_000016.8:g.65757035G>C	NCBI36
NG_009294.1:g.7247G>C
NG_029566.1:g.130G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517867.2:n.515+1G>C
ENST00000523077.2:n.731+1G>C
ENST00000521374.6:c.232+1G>C MANE Select	ENSP00000430947.2:n.232+1G>C
ENST00000434833.6:c.232+1G>C	ENSP00000403219.2:n.232+1G>C
ENST00000517685.5:c.232+1G>C	ENSP00000428978.1:n.232+1G>C
ENST00000517729.5:c.106+1G>C	ENSP00000430299.1:n.106+1G>C
ENST00000518227.1:c.1462G>C
ENST00000518753.5:c.404+1G>C
ENST00000521314.5:c.124-88G>C	ENSP00000429580.1:n.124-88G>C
ENST00000521374.5:c.232+1G>C	ENSP00000430947.1:n.232+1G>C
ENST00000521624.5:c.232+1G>C	ENSP00000428161.1:n.232+1G>C
ENST00000522023.1:n.299+1G>C
ENST00000522295.5:c.232+1G>C	ENSP00000427832.1:n.232+1G>C
ENST00000522870.5:n.364G>C
ENST00000523077.1:n.731+1G>C
ENST00000523562.5:c.232+1G>C	ENSP00000430631.1:n.232+1G>C
ENST00000580114.5:c.1197+1G>C
ENST00000584272.5:c.232+1G>C	ENSP00000463706.1:n.232+1G>C
NM_001040667.2:c.232+1G>C	NP_001035757.1:n.232+1G>C
NM_001538.3:c.232+1G>C	NP_001529.2:n.232+1G>C
NM_001040667.3:c.232+1G>C	NP_001035757.1:n.232+1G>C
NM_001374674.1:c.232+1G>C	NP_001361603.1:n.232+1G>C
NM_001374675.1:c.232+1G>C MANE Select	NP_001361604.1:n.232+1G>C
NM_001538.4:c.232+1G>C	NP_001529.2:n.232+1G>C