Canonical Allele Identifier: CA5239695

Gene: HSPA5

Linked Data

• dbSNP Id: rs757316929
• ExAC: 9:128001138 GTTATC / G
• MyVariant Identifiers: chr9:g.128001139_128001143del (hg19) ; chr9:g.125238860_125238864del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238861_125238865del , CM000671.2:g.125238861_125238865del	GRCh38
NC_000009.11:g.128001140_128001144del , CM000671.1:g.128001140_128001144del	GRCh37
NC_000009.10:g.127040961_127040965del	NCBI36
NG_027761.1:g.7524_7528del

Transcript Alleles

HGVS	Amino-acid change
ENST00000324460.7:c.997-37_997-33del MANE Select	ENSP00000324173.6:n.997-37_997-33del
ENST00000679355.1:n.1315_1319del
ENST00000679475.1:n.1581-37_1581-33del
ENST00000680032.1:c.997-37_997-33del	ENSP00000506285.1:n.997-37_997-33del
ENST00000680234.1:n.1253-37_1253-33del
ENST00000680257.1:n.1253-37_1253-33del
ENST00000680272.1:c.996+77_996+81del	ENSP00000506097.1:n.996+77_996+81del
ENST00000680494.1:n.2384_2388del
ENST00000680640.1:n.1948-37_1948-33del
ENST00000681045.1:n.1877-37_1877-33del
ENST00000681424.1:n.1315_1319del
ENST00000681540.1:n.1253-37_1253-33del
ENST00000681544.1:n.1328-37_1328-33del
ENST00000681675.1:n.1877-37_1877-33del
ENST00000681774.1:n.2219-37_2219-33del
ENST00000324460.6:c.997-37_997-33del	ENSP00000324173.6:n.997-37_997-33del
NM_005347.4:c.997-37_997-33del	NP_005338.1:n.997-37_997-33del
NM_005347.5:c.997-37_997-33del MANE Select	NP_005338.1:n.997-37_997-33del