Canonical Allele Identifier: CA2840041877
Gene: HSPA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125238941del , CM000671.2:g.125238941del GRCh38
NC_000009.11:g.128001220del , CM000671.1:g.128001220del GRCh37
NC_000009.10:g.127041041del NCBI36
NG_027761.1:g.7448del

Transcript Alleles

HGVS Amino-acid Change
ENST00000324460.7:c.996+1del
ENST00000679355.1:n.1239del
ENST00000679475.1:n.1580+1del
ENST00000680032.1:c.996+1del
ENST00000680234.1:n.1252+1del
ENST00000680257.1:n.1252+1del
ENST00000680272.1:c.996+1del
ENST00000680494.1:n.2308del
ENST00000680640.1:n.1947+1del
ENST00000681045.1:n.1876+1del
ENST00000681424.1:n.1239del
ENST00000681540.1:n.1252+1del
ENST00000681544.1:n.1327+1del
ENST00000681675.1:n.1876+1del
ENST00000681774.1:n.2218+1del
ENST00000324460.6:c.996+1del
NM_005347.4:c.996+1del
NM_005347.5:c.996+1del