Canonical Allele Identifier: CA467130230

Gene: HSPA5

Linked Data

• MyVariant Identifiers: chr9:g.128001017A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238738A>T , CM000671.2:g.125238738A>T	GRCh38
NC_000009.11:g.128001017A>T , CM000671.1:g.128001017A>T	GRCh37
NC_000009.10:g.127040838A>T	NCBI36
NG_027761.1:g.7650T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324460.7:c.1086T>A MANE Select	ENSP00000324173.6:p.Val362=
ENST00000679355.1:n.1441T>A
ENST00000679475.1:n.1670T>A
ENST00000680032.1:c.1086T>A	ENSP00000506285.1:p.Val362=
ENST00000680234.1:n.1342T>A
ENST00000680257.1:n.1342T>A
ENST00000680272.1:c.997-25T>A	ENSP00000506097.1:n.997-25T>A
ENST00000680494.1:n.2510T>A
ENST00000680640.1:n.2037T>A
ENST00000681045.1:n.1966T>A
ENST00000681424.1:n.1441T>A
ENST00000681540.1:n.1342T>A
ENST00000681544.1:n.1417T>A
ENST00000681675.1:n.1966T>A
ENST00000681774.1:n.2308T>A
ENST00000324460.6:c.1086T>A	ENSP00000324173.6:p.Val362=
NM_005347.4:c.1086T>A	NP_005338.1:p.Val362=
NM_005347.5:c.1086T>A MANE Select	NP_005338.1:p.Val362=