Canonical Allele Identifier: CA374897476

Gene: HSPA5

Linked Data

• MyVariant Identifiers: chr9:g.128001031C>G (hg19) ; chr9:g.125238752C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238752C>G , CM000671.2:g.125238752C>G	GRCh38
NC_000009.11:g.128001031C>G , CM000671.1:g.128001031C>G	GRCh37
NC_000009.10:g.127040852C>G	NCBI36
NG_027761.1:g.7636G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000324460.7:c.1072G>C MANE Select	ENSP00000324173.6:p.Glu358Gln
ENST00000679355.1:n.1427G>C
ENST00000679475.1:n.1656G>C
ENST00000680032.1:c.1072G>C	ENSP00000506285.1:p.Glu358Gln
ENST00000680234.1:n.1328G>C
ENST00000680257.1:n.1328G>C
ENST00000680272.1:c.997-39G>C	ENSP00000506097.1:n.997-39G>C
ENST00000680494.1:n.2496G>C
ENST00000680640.1:n.2023G>C
ENST00000681045.1:n.1952G>C
ENST00000681424.1:n.1427G>C
ENST00000681540.1:n.1328G>C
ENST00000681544.1:n.1403G>C
ENST00000681675.1:n.1952G>C
ENST00000681774.1:n.2294G>C
ENST00000324460.6:c.1072G>C	ENSP00000324173.6:p.Glu358Gln
NM_005347.4:c.1072G>C	NP_005338.1:p.Glu358Gln
NM_005347.5:c.1072G>C MANE Select	NP_005338.1:p.Glu358Gln