Canonical Allele Identifier: CA374897437

Gene: HSPA5

Linked Data

• gnomAD v4: 9-125238745-A-C
• MyVariant Identifiers: chr9:g.128001024A>C (hg19) ; chr9:g.125238745A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238745A>C , CM000671.2:g.125238745A>C	GRCh38
NC_000009.11:g.128001024A>C , CM000671.1:g.128001024A>C	GRCh37
NC_000009.10:g.127040845A>C	NCBI36
NG_027761.1:g.7643T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000324460.7:c.1079T>G MANE Select	ENSP00000324173.6:p.Val360Gly
ENST00000679355.1:n.1434T>G
ENST00000679475.1:n.1663T>G
ENST00000680032.1:c.1079T>G	ENSP00000506285.1:p.Val360Gly
ENST00000680234.1:n.1335T>G
ENST00000680257.1:n.1335T>G
ENST00000680272.1:c.997-32T>G	ENSP00000506097.1:n.997-32T>G
ENST00000680494.1:n.2503T>G
ENST00000680640.1:n.2030T>G
ENST00000681045.1:n.1959T>G
ENST00000681424.1:n.1434T>G
ENST00000681540.1:n.1335T>G
ENST00000681544.1:n.1410T>G
ENST00000681675.1:n.1959T>G
ENST00000681774.1:n.2301T>G
ENST00000324460.6:c.1079T>G	ENSP00000324173.6:p.Val360Gly
NM_005347.4:c.1079T>G	NP_005338.1:p.Val360Gly
NM_005347.5:c.1079T>G MANE Select	NP_005338.1:p.Val360Gly