Canonical Allele Identifier: CA374897400
Gene: HSPA5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125238731A>C , CM000671.2:g.125238731A>C GRCh38
NC_000009.11:g.128001010A>C , CM000671.1:g.128001010A>C GRCh37
NC_000009.10:g.127040831A>C NCBI36
NG_027761.1:g.7657T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000324460.7:c.1093T>G MANE Select ENSP00000324173.6:p.Ser365Ala
ENST00000679355.1:n.1448T>G
ENST00000679475.1:n.1677T>G
ENST00000680032.1:c.1093T>G ENSP00000506285.1:p.Ser365Ala
ENST00000680234.1:n.1349T>G
ENST00000680257.1:n.1349T>G
ENST00000680272.1:c.997-18T>G ENSP00000506097.1:n.997-18T>G
ENST00000680494.1:n.2517T>G
ENST00000680640.1:n.2044T>G
ENST00000681045.1:n.1973T>G
ENST00000681424.1:n.1448T>G
ENST00000681540.1:n.1349T>G
ENST00000681544.1:n.1424T>G
ENST00000681675.1:n.1973T>G
ENST00000681774.1:n.2315T>G
ENST00000324460.6:c.1093T>G ENSP00000324173.6:p.Ser365Ala
NM_005347.4:c.1093T>G NP_005338.1:p.Ser365Ala
NM_005347.5:c.1093T>G MANE Select NP_005338.1:p.Ser365Ala