Canonical Allele Identifier: CA353421

Gene: HSPA9

Linked Data

• ClinVar Variation Id: 224070
• ClinVar RCV Id: RCV000209862
• dbSNP Id: rs869312659
• MyVariant Identifiers: chr5:g.137895585_137895590del (hg19) ; chr5:g.138559896_138559901del (hg38)
• PubMed: PMID:26491070

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138559898_138559903del , CM000667.2:g.138559898_138559903del	GRCh38
NC_000005.9:g.137895587_137895592del , CM000667.1:g.137895587_137895592del	GRCh37
NC_000005.8:g.137923486_137923491del	NCBI36
NG_029469.1:g.20729_20734del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297185.9:c.1373_1378del MANE Select	ENSP00000297185.3:p.Ile458_Asn459del
ENST00000501917.7:n.104-4360_104-4355del
ENST00000504902.6:c.*147_*152del	ENSP00000421311.2:n.*147_*152del
ENST00000507115.6:c.1373_1378del	ENSP00000423759.2:p.Ile458_Asn459del
ENST00000508003.2:n.1474_1479del
ENST00000524109.2:n.1730_1735del
ENST00000649578.2:c.*756_*761del	ENSP00000497906.1:n.*756_*761del
ENST00000649692.2:n.2964_2969del
ENST00000677064.1:c.1183-1244_1183-1239del	ENSP00000503373.1:n.1183-1244_1183-1239del
ENST00000677066.1:c.1166_1171del	ENSP00000502902.1:p.Ile389_Asn390del
ENST00000677425.1:c.1280_1285del	ENSP00000503066.1:p.Ile427_Asn428del
ENST00000677527.1:c.*1197_*1202del	ENSP00000503650.1:n.*1197_*1202del
ENST00000677553.1:c.1368_1373del	ENSP00000502970.1:n.1368_1373del
ENST00000677693.1:c.*1287_*1292del	ENSP00000503383.1:n.*1287_*1292del
ENST00000677988.1:c.*1287_*1292del	ENSP00000502960.1:n.*1287_*1292del
ENST00000678051.1:c.1067_1072del	ENSP00000503219.1:p.Ile356_Asn357del
ENST00000678300.1:c.1166_1171del	ENSP00000503259.1:p.Ile389_Asn390del
ENST00000678384.1:c.1166_1171del	ENSP00000503992.1:p.Ile389_Asn390del
ENST00000678551.1:n.1476_1481del
ENST00000678794.1:c.1381_1386del
ENST00000297185.7:c.1373_1378del	ENSP00000297185.3:p.Ile458_Asn459del
ENST00000501917.6:n.94-4360_94-4355del
ENST00000507097.5:n.1499_1504del
ENST00000508003.1:n.401_406del
ENST00000523929.1:c.638_643del
NM_004134.6:c.1373_1378del	NP_004125.3:p.Ile458_Asn459del
XR_948819.1:n.74+16494_74+16499del
NM_004134.7:c.1373_1378del MANE Select	NP_004125.3:p.Ile458_Asn459del