Canonical Allele Identifier: CA374897214

Gene: HSPA5

Linked Data

• dbSNP Id: rs1832526471
• MyVariant Identifiers: chr9:g.128000965T>C (hg19) ; chr9:g.125238686T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238686T>C , CM000671.2:g.125238686T>C	GRCh38
NC_000009.11:g.128000965T>C , CM000671.1:g.128000965T>C	GRCh37
NC_000009.10:g.127040786T>C	NCBI36
NG_027761.1:g.7702A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324460.7:c.1138A>G MANE Select	ENSP00000324173.6:p.Asn380Asp
ENST00000679355.1:n.1493A>G
ENST00000679475.1:n.1722A>G
ENST00000680032.1:c.1138A>G	ENSP00000506285.1:p.Asn380Asp
ENST00000680234.1:n.1394A>G
ENST00000680257.1:n.1394A>G
ENST00000680272.1:c.1024A>G	ENSP00000506097.1:p.Asn342Asp
ENST00000680494.1:n.2562A>G
ENST00000680640.1:n.2089A>G
ENST00000681045.1:n.2018A>G
ENST00000681424.1:n.1493A>G
ENST00000681540.1:n.1394A>G
ENST00000681544.1:n.1469A>G
ENST00000681675.1:n.2018A>G
ENST00000681774.1:n.2360A>G
ENST00000324460.6:c.1138A>G	ENSP00000324173.6:p.Asn380Asp
NM_005347.4:c.1138A>G	NP_005338.1:p.Asn380Asp
NM_005347.5:c.1138A>G MANE Select	NP_005338.1:p.Asn380Asp