Canonical Allele Identifier: CA1878829825
Gene: HSPA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125238751T= , CM000671.2:g.125238751T= GRCh38
NC_000009.11:g.128001030T= , CM000671.1:g.128001030T= GRCh37
NC_000009.10:g.127040851T= NCBI36
NG_027761.1:g.7637A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000324460.7:c.1073A= MANE Select ENSP00000324173.6:p.Glu358=
ENST00000679355.1:n.1428A=
ENST00000679475.1:n.1657A=
ENST00000680032.1:c.1073A= ENSP00000506285.1:p.Glu358=
ENST00000680234.1:n.1329A=
ENST00000680257.1:n.1329A=
ENST00000680272.1:c.997-38A= ENSP00000506097.1:n.997-38A=
ENST00000680494.1:n.2497A=
ENST00000680640.1:n.2024A=
ENST00000681045.1:n.1953A=
ENST00000681424.1:n.1428A=
ENST00000681540.1:n.1329A=
ENST00000681544.1:n.1404A=
ENST00000681675.1:n.1953A=
ENST00000681774.1:n.2295A=
ENST00000324460.6:c.1073A= ENSP00000324173.6:p.Glu358=
NM_005347.4:c.1073A= NP_005338.1:p.Glu358=
NM_005347.5:c.1073A= MANE Select NP_005338.1:p.Glu358=