Canonical Allele Identifier: CA5239689

Gene: HSPA5

Linked Data

• dbSNP Id: rs771120515
• ExAC: 9:128001123 G / C
• gnomAD v2: 9-128001123-G-C
• gnomAD v4: 9-125238844-G-C
• MyVariant Identifiers: chr9:g.128001123G>C (hg19) ; chr9:g.125238844G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238844G>C , CM000671.2:g.125238844G>C	GRCh38
NC_000009.11:g.128001123G>C , CM000671.1:g.128001123G>C	GRCh37
NC_000009.10:g.127040944G>C	NCBI36
NG_027761.1:g.7544C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000324460.7:c.997-17C>G MANE Select	ENSP00000324173.6:n.997-17C>G
ENST00000679355.1:n.1335C>G
ENST00000679475.1:n.1581-17C>G
ENST00000680032.1:c.997-17C>G	ENSP00000506285.1:n.997-17C>G
ENST00000680234.1:n.1253-17C>G
ENST00000680257.1:n.1253-17C>G
ENST00000680272.1:c.996+97C>G	ENSP00000506097.1:n.996+97C>G
ENST00000680494.1:n.2404C>G
ENST00000680640.1:n.1948-17C>G
ENST00000681045.1:n.1877-17C>G
ENST00000681424.1:n.1335C>G
ENST00000681540.1:n.1253-17C>G
ENST00000681544.1:n.1328-17C>G
ENST00000681675.1:n.1877-17C>G
ENST00000681774.1:n.2219-17C>G
ENST00000324460.6:c.997-17C>G	ENSP00000324173.6:n.997-17C>G
NM_005347.4:c.997-17C>G	NP_005338.1:n.997-17C>G
NM_005347.5:c.997-17C>G MANE Select	NP_005338.1:n.997-17C>G