Canonical Allele Identifier: CA467209571

Gene: HSPA5

Linked Data

• MyVariant Identifiers: chr9:g.128001089A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238810A>T , CM000671.2:g.125238810A>T	GRCh38
NC_000009.11:g.128001089A>T , CM000671.1:g.128001089A>T	GRCh37
NC_000009.10:g.127040910A>T	NCBI36
NG_027761.1:g.7578T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324460.7:c.1014T>A MANE Select	ENSP00000324173.6:p.Thr338=
ENST00000679355.1:n.1369T>A
ENST00000679475.1:n.1598T>A
ENST00000680032.1:c.1014T>A	ENSP00000506285.1:p.Thr338=
ENST00000680234.1:n.1270T>A
ENST00000680257.1:n.1270T>A
ENST00000680272.1:c.997-97T>A	ENSP00000506097.1:n.997-97T>A
ENST00000680494.1:n.2438T>A
ENST00000680640.1:n.1965T>A
ENST00000681045.1:n.1894T>A
ENST00000681424.1:n.1369T>A
ENST00000681540.1:n.1270T>A
ENST00000681544.1:n.1345T>A
ENST00000681675.1:n.1894T>A
ENST00000681774.1:n.2236T>A
ENST00000324460.6:c.1014T>A	ENSP00000324173.6:p.Thr338=
NM_005347.4:c.1014T>A	NP_005338.1:p.Thr338=
NM_005347.5:c.1014T>A MANE Select	NP_005338.1:p.Thr338=