Canonical Allele Identifier: CA2579451906

Gene: HSPA5

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238866_125238872del , CM000671.2:g.125238866_125238872del	GRCh38
NC_000009.11:g.128001145_128001151del , CM000671.1:g.128001145_128001151del	GRCh37
NC_000009.10:g.127040966_127040972del	NCBI36
NG_027761.1:g.7516_7522del

Transcript Alleles

HGVS	Amino-acid change
ENST00000324460.7:c.997-45_997-39del MANE Select	ENSP00000324173.6:n.997-45_997-39del
ENST00000679355.1:n.1307_1313del
ENST00000679475.1:n.1581-45_1581-39del
ENST00000680032.1:c.997-45_997-39del	ENSP00000506285.1:n.997-45_997-39del
ENST00000680234.1:n.1253-45_1253-39del
ENST00000680257.1:n.1253-45_1253-39del
ENST00000680272.1:c.996+69_996+75del	ENSP00000506097.1:n.996+69_996+75del
ENST00000680494.1:n.2376_2382del
ENST00000680640.1:n.1948-45_1948-39del
ENST00000681045.1:n.1877-45_1877-39del
ENST00000681424.1:n.1307_1313del
ENST00000681540.1:n.1253-45_1253-39del
ENST00000681544.1:n.1328-45_1328-39del
ENST00000681675.1:n.1877-45_1877-39del
ENST00000681774.1:n.2219-45_2219-39del
ENST00000324460.6:c.997-45_997-39del	ENSP00000324173.6:n.997-45_997-39del
NM_005347.4:c.997-45_997-39del	NP_005338.1:n.997-45_997-39del
NM_005347.5:c.997-45_997-39del MANE Select	NP_005338.1:n.997-45_997-39del