Canonical Allele Identifier: CA374897053

Gene: HSPA5

Linked Data

• MyVariant Identifiers: chr9:g.128000931T>C (hg19) ; chr9:g.125238652T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238652T>C , CM000671.2:g.125238652T>C	GRCh38
NC_000009.11:g.128000931T>C , CM000671.1:g.128000931T>C	GRCh37
NC_000009.10:g.127040752T>C	NCBI36
NG_027761.1:g.7736A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324460.7:c.1172A>G MANE Select	ENSP00000324173.6:p.Asp391Gly
ENST00000679355.1:n.1527A>G
ENST00000679475.1:n.1756A>G
ENST00000680032.1:c.1172A>G	ENSP00000506285.1:p.Asp391Gly
ENST00000680234.1:n.1428A>G
ENST00000680257.1:n.1428A>G
ENST00000680272.1:c.1058A>G	ENSP00000506097.1:p.Asp353Gly
ENST00000680494.1:n.2596A>G
ENST00000680640.1:n.2123A>G
ENST00000681045.1:n.2052A>G
ENST00000681424.1:n.1527A>G
ENST00000681540.1:n.1428A>G
ENST00000681544.1:n.1503A>G
ENST00000681675.1:n.2052A>G
ENST00000681774.1:n.2394A>G
ENST00000324460.6:c.1172A>G	ENSP00000324173.6:p.Asp391Gly
NM_005347.4:c.1172A>G	NP_005338.1:p.Asp391Gly
NM_005347.5:c.1172A>G MANE Select	NP_005338.1:p.Asp391Gly