Canonical Allele Identifier: CA467209664

Gene: HSPA5

Linked Data

• gnomAD v4: 9-125238965-C-T
• MyVariant Identifiers: chr9:g.128001244C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238965C>T , CM000671.2:g.125238965C>T	GRCh38
NC_000009.11:g.128001244C>T , CM000671.1:g.128001244C>T	GRCh37
NC_000009.10:g.127041065C>T	NCBI36
NG_027761.1:g.7423G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324460.7:c.972G>A MANE Select	ENSP00000324173.6:p.Arg324=
ENST00000679355.1:n.1214G>A
ENST00000679475.1:n.1556G>A
ENST00000680032.1:c.972G>A	ENSP00000506285.1:p.Arg324=
ENST00000680234.1:n.1228G>A
ENST00000680257.1:n.1228G>A
ENST00000680272.1:c.972G>A	ENSP00000506097.1:p.Arg324=
ENST00000680494.1:n.2283G>A
ENST00000680640.1:n.1923G>A
ENST00000681045.1:n.1852G>A
ENST00000681424.1:n.1214G>A
ENST00000681540.1:n.1228G>A
ENST00000681544.1:n.1303G>A
ENST00000681675.1:n.1852G>A
ENST00000681774.1:n.2194G>A
ENST00000324460.6:c.972G>A	ENSP00000324173.6:p.Arg324=
NM_005347.4:c.972G>A	NP_005338.1:p.Arg324=
NM_005347.5:c.972G>A MANE Select	NP_005338.1:p.Arg324=