Canonical Allele Identifier: CA199744806

Gene: HSPA5

Linked Data

• dbSNP Id: rs866597853
• MyVariant Identifiers: chr9:g.128001243C>T (hg19) ; chr9:g.125238964C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238964C>T , CM000671.2:g.125238964C>T	GRCh38
NC_000009.11:g.128001243C>T , CM000671.1:g.128001243C>T	GRCh37
NC_000009.10:g.127041064C>T	NCBI36
NG_027761.1:g.7424G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324460.7:c.973G>A MANE Select	ENSP00000324173.6:p.Ala325Thr
ENST00000679355.1:n.1215G>A
ENST00000679475.1:n.1557G>A
ENST00000680032.1:c.973G>A	ENSP00000506285.1:p.Ala325Thr
ENST00000680234.1:n.1229G>A
ENST00000680257.1:n.1229G>A
ENST00000680272.1:c.973G>A	ENSP00000506097.1:p.Ala325Thr
ENST00000680494.1:n.2284G>A
ENST00000680640.1:n.1924G>A
ENST00000681045.1:n.1853G>A
ENST00000681424.1:n.1215G>A
ENST00000681540.1:n.1229G>A
ENST00000681544.1:n.1304G>A
ENST00000681675.1:n.1853G>A
ENST00000681774.1:n.2195G>A
ENST00000324460.6:c.973G>A	ENSP00000324173.6:p.Ala325Thr
NM_005347.4:c.973G>A	NP_005338.1:p.Ala325Thr
NM_005347.5:c.973G>A MANE Select	NP_005338.1:p.Ala325Thr