Canonical Allele Identifier: CA1878829813
Gene: HSPA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125238741A= , CM000671.2:g.125238741A= GRCh38
NC_000009.11:g.128001020A= , CM000671.1:g.128001020A= GRCh37
NC_000009.10:g.127040841A= NCBI36
NG_027761.1:g.7647T=

Transcript Alleles

HGVS Amino-acid change
ENST00000324460.7:c.1083T= MANE Select ENSP00000324173.6:p.Leu361=
ENST00000679355.1:n.1438T=
ENST00000679475.1:n.1667T=
ENST00000680032.1:c.1083T= ENSP00000506285.1:p.Leu361=
ENST00000680234.1:n.1339T=
ENST00000680257.1:n.1339T=
ENST00000680272.1:c.997-28T= ENSP00000506097.1:n.997-28T=
ENST00000680494.1:n.2507T=
ENST00000680640.1:n.2034T=
ENST00000681045.1:n.1963T=
ENST00000681424.1:n.1438T=
ENST00000681540.1:n.1339T=
ENST00000681544.1:n.1414T=
ENST00000681675.1:n.1963T=
ENST00000681774.1:n.2305T=
ENST00000324460.6:c.1083T= ENSP00000324173.6:p.Leu361=
NM_005347.4:c.1083T= NP_005338.1:p.Leu361=
NM_005347.5:c.1083T= MANE Select NP_005338.1:p.Leu361=