Canonical Allele Identifier: CA374897834

Gene: HSPA5

Linked Data

• gnomAD v4: 9-125238827-C-A
• MyVariant Identifiers: chr9:g.128001106C>A (hg19) ; chr9:g.125238827C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238827C>A , CM000671.2:g.125238827C>A	GRCh38
NC_000009.11:g.128001106C>A , CM000671.1:g.128001106C>A	GRCh37
NC_000009.10:g.127040927C>A	NCBI36
NG_027761.1:g.7561G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324460.7:c.997G>T MANE Select	ENSP00000324173.6:p.Asp333Tyr
ENST00000679355.1:n.1352G>T
ENST00000679475.1:n.1581G>T
ENST00000680032.1:c.997G>T	ENSP00000506285.1:p.Asp333Tyr
ENST00000680234.1:n.1253G>T
ENST00000680257.1:n.1253G>T
ENST00000680272.1:c.997-114G>T	ENSP00000506097.1:n.997-114G>T
ENST00000680494.1:n.2421G>T
ENST00000680640.1:n.1948G>T
ENST00000681045.1:n.1877G>T
ENST00000681424.1:n.1352G>T
ENST00000681540.1:n.1253G>T
ENST00000681544.1:n.1328G>T
ENST00000681675.1:n.1877G>T
ENST00000681774.1:n.2219G>T
ENST00000324460.6:c.997G>T	ENSP00000324173.6:p.Asp333Tyr
NM_005347.4:c.997G>T	NP_005338.1:p.Asp333Tyr
NM_005347.5:c.997G>T MANE Select	NP_005338.1:p.Asp333Tyr