Canonical Allele Identifier: CA2616532888

Gene: HSPA8

Linked Data

• gnomAD v4: 11-123059123-ATGGTGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059125_123059130del , CM000673.2:g.123059125_123059130del	GRCh38
NC_000011.9:g.122929833_122929838del , CM000673.1:g.122929833_122929838del	GRCh37
NC_000011.8:g.122435043_122435048del	NCBI36
NG_029473.1:g.8008_8013del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1253_1258del MANE Select	ENSP00000432083.1:p.Thr418_Thr419del
ENST00000227378.7:c.1253_1258del	ENSP00000227378.3:p.Thr418_Thr419del
ENST00000453788.6:c.1253_1258del	ENSP00000404372.2:p.Thr418_Thr419del
ENST00000524552.5:c.26_31del	ENSP00000435908.1:p.Thr9_Thr10del
ENST00000526110.5:c.1196_1201del	ENSP00000433584.1:p.Thr399_Thr400del
ENST00000532091.1:n.1000_1005del
ENST00000532636.5:c.1253_1258del	ENSP00000437125.1:p.Thr418_Thr419del
ENST00000533238.5:n.381-26_381-21del
ENST00000533540.5:c.815_820del	ENSP00000437189.1:p.Thr272_Thr273del
ENST00000534319.5:c.545_550del	ENSP00000433316.1:p.Thr182_Thr183del
ENST00000534624.5:c.1253_1258del	ENSP00000432083.1:p.Thr418_Thr419del
NM_006597.5:c.1253_1258del	NP_006588.1:p.Thr418_Thr419del
NM_153201.3:c.1253_1258del	NP_694881.1:p.Thr418_Thr419del
XM_011542798.1:c.1253_1258del	XP_011541100.1:p.Thr418_Thr419del
NM_006597.6:c.1253_1258del MANE Select	NP_006588.1:p.Thr418_Thr419del
NM_153201.4:c.1253_1258del	NP_694881.1:p.Thr418_Thr419del