Canonical Allele Identifier: CA199744812

Gene: HSPA5

Linked Data

• dbSNP Id: rs762582529
• gnomAD v4: 9-125238966-C-T
• COSMIC: COSM6285145
• MyVariant Identifiers: chr9:g.128001245C>T (hg19) ; chr9:g.125238966C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238966C>T , CM000671.2:g.125238966C>T	GRCh38
NC_000009.11:g.128001245C>T , CM000671.1:g.128001245C>T	GRCh37
NC_000009.10:g.127041066C>T	NCBI36
NG_027761.1:g.7422G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324460.7:c.971G>A MANE Select	ENSP00000324173.6:p.Arg324Gln
ENST00000679355.1:n.1213G>A
ENST00000679475.1:n.1555G>A
ENST00000680032.1:c.971G>A	ENSP00000506285.1:p.Arg324Gln
ENST00000680234.1:n.1227G>A
ENST00000680257.1:n.1227G>A
ENST00000680272.1:c.971G>A	ENSP00000506097.1:p.Arg324Gln
ENST00000680494.1:n.2282G>A
ENST00000680640.1:n.1922G>A
ENST00000681045.1:n.1851G>A
ENST00000681424.1:n.1213G>A
ENST00000681540.1:n.1227G>A
ENST00000681544.1:n.1302G>A
ENST00000681675.1:n.1851G>A
ENST00000681774.1:n.2193G>A
ENST00000324460.6:c.971G>A	ENSP00000324173.6:p.Arg324Gln
NM_005347.4:c.971G>A	NP_005338.1:p.Arg324Gln
NM_005347.5:c.971G>A MANE Select	NP_005338.1:p.Arg324Gln