Canonical Allele Identifier: CA3431008

Gene: HSPA9

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138567189del , CM000667.2:g.138567189del	GRCh38
NC_000005.9:g.137902878del , CM000667.1:g.137902878del	GRCh37
NC_000005.8:g.137930777del	NCBI36
NG_029469.1:g.13450del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297185.9:c.717-17del MANE Select	ENSP00000297185.3:n.717-17del
ENST00000504902.6:c.717-17del	ENSP00000421311.2:n.717-17del
ENST00000507115.6:c.717-17del	ENSP00000423759.2:n.717-17del
ENST00000508003.2:n.818-17del
ENST00000524109.2:n.1074-17del
ENST00000649578.2:c.*100-17del	ENSP00000497906.1:n.*100-17del
ENST00000649692.2:n.820-17del
ENST00000677064.1:c.717-17del	ENSP00000503373.1:n.717-17del
ENST00000677066.1:c.510-17del	ENSP00000502902.1:n.510-17del
ENST00000677425.1:c.717-17del	ENSP00000503066.1:n.717-17del
ENST00000677527.1:c.*541-17del	ENSP00000503650.1:n.*541-17del
ENST00000677553.1:c.712-17del	ENSP00000502970.1:n.712-17del
ENST00000677693.1:c.*631-17del	ENSP00000503383.1:n.*631-17del
ENST00000677988.1:c.*631-17del	ENSP00000502960.1:n.*631-17del
ENST00000678051.1:c.411-17del	ENSP00000503219.1:n.411-17del
ENST00000678300.1:c.510-17del	ENSP00000503259.1:n.510-17del
ENST00000678384.1:c.510-17del	ENSP00000503992.1:n.510-17del
ENST00000678551.1:n.820-17del
ENST00000678794.1:c.725-17del
ENST00000297185.7:c.717-17del	ENSP00000297185.3:n.717-17del
ENST00000504902.5:c.725-17del
ENST00000507097.5:n.843-17del
NM_004134.6:c.717-17del	NP_004125.3:n.717-17del
XR_948819.1:n.75-16639del
NM_004134.7:c.717-17del MANE Select	NP_004125.3:n.717-17del