Canonical Allele Identifier: CA723022149

Gene: HSF4

Linked Data

• dbSNP Id: rs774126868
• MyVariant Identifiers: chr16:g.67198682G>C (hg19) ; chr16:g.67164779G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67164779G>C , CM000678.2:g.67164779G>C	GRCh38
NC_000016.9:g.67198682G>C , CM000678.1:g.67198682G>C	GRCh37
NC_000016.8:g.65756183G>C	NCBI36
NG_009294.1:g.6395G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521374.6:c.-33G>C MANE Select	ENSP00000430947.2:n.-33G>C
ENST00000434833.6:c.-33G>C	ENSP00000403219.2:n.-33G>C
ENST00000518227.1:c.610G>C
ENST00000518753.5:c.295+635G>C
ENST00000521314.5:c.-33G>C	ENSP00000429580.1:n.-33G>C
ENST00000522023.1:n.35G>C
ENST00000522295.5:c.-33G>C	ENSP00000427832.1:n.-33G>C
ENST00000522870.5:n.99G>C
ENST00000523360.1:n.459G>C
ENST00000580114.5:c.933G>C
NM_001040667.2:c.-33G>C	NP_001035757.1:n.-33G>C
NM_001538.3:c.-33G>C	NP_001529.2:n.-33G>C
NM_001040667.3:c.-33G>C	NP_001035757.1:n.-33G>C
NM_001374674.1:c.-33G>C	NP_001361603.1:n.-33G>C
NM_001374675.1:c.-33G>C MANE Select	NP_001361604.1:n.-33G>C
NM_001538.4:c.-33G>C	NP_001529.2:n.-33G>C