Canonical Allele Identifier: CA5239688

Gene: HSPA5

Linked Data

• dbSNP Id: rs747246754
• ExAC: 9:128001121 T / C
• gnomAD v2: 9-128001121-T-C
• gnomAD v4: 9-125238842-T-C
• MyVariant Identifiers: chr9:g.128001121T>C (hg19) ; chr9:g.125238842T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238842T>C , CM000671.2:g.125238842T>C	GRCh38
NC_000009.11:g.128001121T>C , CM000671.1:g.128001121T>C	GRCh37
NC_000009.10:g.127040942T>C	NCBI36
NG_027761.1:g.7546A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324460.7:c.997-15A>G MANE Select	ENSP00000324173.6:n.997-15A>G
ENST00000679355.1:n.1337A>G
ENST00000679475.1:n.1581-15A>G
ENST00000680032.1:c.997-15A>G	ENSP00000506285.1:n.997-15A>G
ENST00000680234.1:n.1253-15A>G
ENST00000680257.1:n.1253-15A>G
ENST00000680272.1:c.996+99A>G	ENSP00000506097.1:n.996+99A>G
ENST00000680494.1:n.2406A>G
ENST00000680640.1:n.1948-15A>G
ENST00000681045.1:n.1877-15A>G
ENST00000681424.1:n.1337A>G
ENST00000681540.1:n.1253-15A>G
ENST00000681544.1:n.1328-15A>G
ENST00000681675.1:n.1877-15A>G
ENST00000681774.1:n.2219-15A>G
ENST00000324460.6:c.997-15A>G	ENSP00000324173.6:n.997-15A>G
NM_005347.4:c.997-15A>G	NP_005338.1:n.997-15A>G
NM_005347.5:c.997-15A>G MANE Select	NP_005338.1:n.997-15A>G