Canonical Allele Identifier: CA590937476

Gene: HSPA5

Linked Data

• dbSNP Id: rs1564207384
• gnomAD v2: 9-128001136-CT-C
• gnomAD v3: 9-125238857-CT-C
• gnomAD v4: 9-125238857-CT-C
• MyVariant Identifiers: chr9:g.128001137del (hg19) ; chr9:g.125238858del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238858del , CM000671.2:g.125238858del	GRCh38
NC_000009.11:g.128001137del , CM000671.1:g.128001137del	GRCh37
NC_000009.10:g.127040958del	NCBI36
NG_027761.1:g.7530del

Transcript Alleles

HGVS	Amino-acid change
ENST00000324460.7:c.997-31del MANE Select	ENSP00000324173.6:n.997-31del
ENST00000679355.1:n.1321del
ENST00000679475.1:n.1581-31del
ENST00000680032.1:c.997-31del	ENSP00000506285.1:n.997-31del
ENST00000680234.1:n.1253-31del
ENST00000680257.1:n.1253-31del
ENST00000680272.1:c.996+83del	ENSP00000506097.1:n.996+83del
ENST00000680494.1:n.2390del
ENST00000680640.1:n.1948-31del
ENST00000681045.1:n.1877-31del
ENST00000681424.1:n.1321del
ENST00000681540.1:n.1253-31del
ENST00000681544.1:n.1328-31del
ENST00000681675.1:n.1877-31del
ENST00000681774.1:n.2219-31del
ENST00000324460.6:c.997-31del	ENSP00000324173.6:n.997-31del
NM_005347.4:c.997-31del	NP_005338.1:n.997-31del
NM_005347.5:c.997-31del MANE Select	NP_005338.1:n.997-31del