Canonical Allele Identifier: CA212266

Gene: HSPA9

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138570987T>C , CM000667.2:g.138570987T>C	GRCh38
NC_000005.9:g.137906676T>C , CM000667.1:g.137906676T>C	GRCh37
NC_000005.8:g.137934575T>C	NCBI36
NG_029469.1:g.9643A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297185.9:c.383A>G MANE Select	ENSP00000297185.3:p.Tyr128Cys
ENST00000504902.6:c.383A>G	ENSP00000421311.2:p.Tyr128Cys
ENST00000507115.6:c.383A>G	ENSP00000423759.2:p.Tyr128Cys
ENST00000508003.2:n.484A>G
ENST00000524109.2:n.740A>G
ENST00000649578.2:c.383A>G	ENSP00000497906.1:p.Tyr128Cys
ENST00000649692.2:n.486A>G
ENST00000677064.1:c.383A>G	ENSP00000503373.1:p.Tyr128Cys
ENST00000677066.1:c.176A>G	ENSP00000502902.1:p.Tyr59Cys
ENST00000677425.1:c.383A>G	ENSP00000503066.1:p.Tyr128Cys
ENST00000677527.1:c.*207A>G	ENSP00000503650.1:n.*207A>G
ENST00000677553.1:c.378A>G	ENSP00000502970.1:n.378A>G
ENST00000677693.1:c.*297A>G	ENSP00000503383.1:n.*297A>G
ENST00000677988.1:c.*297A>G	ENSP00000502960.1:n.*297A>G
ENST00000678051.1:c.77A>G	ENSP00000503219.1:p.Tyr26Cys
ENST00000678300.1:c.176A>G	ENSP00000503259.1:p.Tyr59Cys
ENST00000678384.1:c.176A>G	ENSP00000503992.1:p.Tyr59Cys
ENST00000678551.1:n.486A>G
ENST00000678794.1:c.391A>G
ENST00000297185.7:c.383A>G	ENSP00000297185.3:p.Tyr128Cys
ENST00000504810.5:c.176A>G	ENSP00000425598.1:p.Tyr59Cys
ENST00000504902.5:c.391A>G
ENST00000505110.1:c.*207A>G	ENSP00000420944.1:n.*207A>G
ENST00000506477.5:n.476A>G
ENST00000507097.5:n.509A>G
ENST00000507115.5:c.*297A>G	ENSP00000423759.1:n.*297A>G
ENST00000507886.1:c.176A>G	ENSP00000423098.1:p.Tyr59Cys
NM_004134.6:c.383A>G	NP_004125.3:p.Tyr128Cys
XR_948819.1:n.75-12841T>C
NM_004134.7:c.383A>G MANE Select	NP_004125.3:p.Tyr128Cys