Canonical Allele Identifier: CA374897045

Gene: HSPA5

Linked Data

• MyVariant Identifiers: chr9:g.128000929C>T (hg19) ; chr9:g.125238650C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238650C>T , CM000671.2:g.125238650C>T	GRCh38
NC_000009.11:g.128000929C>T , CM000671.1:g.128000929C>T	GRCh37
NC_000009.10:g.127040750C>T	NCBI36
NG_027761.1:g.7738G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324460.7:c.1174G>A MANE Select	ENSP00000324173.6:p.Glu392Lys
ENST00000679355.1:n.1529G>A
ENST00000679475.1:n.1758G>A
ENST00000680032.1:c.1174G>A	ENSP00000506285.1:p.Glu392Lys
ENST00000680234.1:n.1430G>A
ENST00000680257.1:n.1430G>A
ENST00000680272.1:c.1060G>A	ENSP00000506097.1:p.Glu354Lys
ENST00000680494.1:n.2598G>A
ENST00000680640.1:n.2125G>A
ENST00000681045.1:n.2054G>A
ENST00000681424.1:n.1529G>A
ENST00000681540.1:n.1430G>A
ENST00000681544.1:n.1505G>A
ENST00000681675.1:n.2054G>A
ENST00000681774.1:n.2396G>A
ENST00000324460.6:c.1174G>A	ENSP00000324173.6:p.Glu392Lys
NM_005347.4:c.1174G>A	NP_005338.1:p.Glu392Lys
NM_005347.5:c.1174G>A MANE Select	NP_005338.1:p.Glu392Lys