Canonical Allele Identifier: CA2005596982
Gene: HSPA8 HGNC NCBI

Linked Data

dbSNP Id: rs1865413875

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.123059180_123059181insTTCT , CM000673.2:g.123059180_123059181insTTCT GRCh38
NC_000011.9:g.122929888_122929889insTTCT , CM000673.1:g.122929888_122929889insTTCT GRCh37
NC_000011.8:g.122435098_122435099insTTCT NCBI36
NG_029473.1:g.7956_7957insAGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000534624.6:c.1201_1202insAGAA MANE Select ENSP00000432083.1:p.Leu401GlnfsTer5
ENST00000227378.7:c.1201_1202insAGAA ENSP00000227378.3:p.Leu401GlnfsTer5
ENST00000453788.6:c.1201_1202insAGAA ENSP00000404372.2:p.Leu401GlnfsTer5
ENST00000524552.5:c.-27_-26insAGAA ENSP00000435908.1:n.-27_-26insAGAA
ENST00000526110.5:c.1144_1145insAGAA ENSP00000433584.1:p.Leu382GlnfsTer5
ENST00000526862.1:n.479_480insAGAA
ENST00000532091.1:n.948_949insAGAA
ENST00000532636.5:c.1201_1202insAGAA ENSP00000437125.1:p.Leu401GlnfsTer5
ENST00000533238.5:n.381-78_381-77insAGAA
ENST00000533540.5:c.763_764insAGAA ENSP00000437189.1:p.Leu255GlnfsTer5
ENST00000534319.5:c.493_494insAGAA ENSP00000433316.1:p.Leu165GlnfsTer5
ENST00000534624.5:c.1201_1202insAGAA ENSP00000432083.1:p.Leu401GlnfsTer5
NM_006597.5:c.1201_1202insAGAA NP_006588.1:p.Leu401GlnfsTer5
NM_153201.3:c.1201_1202insAGAA NP_694881.1:p.Leu401GlnfsTer5
XM_011542798.1:c.1201_1202insAGAA XP_011541100.1:p.Leu401GlnfsTer5
NM_006597.6:c.1201_1202insAGAA MANE Select NP_006588.1:p.Leu401GlnfsTer5
NM_153201.4:c.1201_1202insAGAA NP_694881.1:p.Leu401GlnfsTer5