Canonical Allele Identifier: CA467130059

Gene: HSPA5

Linked Data

• gnomAD v4: 9-125238681-G-A
• MyVariant Identifiers: chr9:g.128000960G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238681G>A , CM000671.2:g.125238681G>A	GRCh38
NC_000009.11:g.128000960G>A , CM000671.1:g.128000960G>A	GRCh37
NC_000009.10:g.127040781G>A	NCBI36
NG_027761.1:g.7707C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324460.7:c.1143C>T MANE Select	ENSP00000324173.6:p.Gly381=
ENST00000679355.1:n.1498C>T
ENST00000679475.1:n.1727C>T
ENST00000680032.1:c.1143C>T	ENSP00000506285.1:p.Gly381=
ENST00000680234.1:n.1399C>T
ENST00000680257.1:n.1399C>T
ENST00000680272.1:c.1029C>T	ENSP00000506097.1:p.Gly343=
ENST00000680494.1:n.2567C>T
ENST00000680640.1:n.2094C>T
ENST00000681045.1:n.2023C>T
ENST00000681424.1:n.1498C>T
ENST00000681540.1:n.1399C>T
ENST00000681544.1:n.1474C>T
ENST00000681675.1:n.2023C>T
ENST00000681774.1:n.2365C>T
ENST00000324460.6:c.1143C>T	ENSP00000324173.6:p.Gly381=
NM_005347.4:c.1143C>T	NP_005338.1:p.Gly381=
NM_005347.5:c.1143C>T MANE Select	NP_005338.1:p.Gly381=