Canonical Allele Identifier: CA2575011573
Gene: HSPA8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.123058633del , CM000673.2:g.123058633del GRCh38
NC_000011.9:g.122929341del , CM000673.1:g.122929341del GRCh37
NC_000011.8:g.122434551del NCBI36
NG_029473.1:g.8506del

Transcript Alleles

HGVS Amino-acid Change
ENST00000534624.6:c.1522+1del
ENST00000227378.7:c.1522+1del
ENST00000453788.6:c.1387+136del ENSP00000404372.2:n.1387+136del
ENST00000524552.5:c.295+1del
ENST00000526110.5:c.1465+1del
ENST00000526686.1:c.178+1del
ENST00000532091.1:n.1498del
ENST00000532636.5:c.1522+1del
ENST00000533540.5:c.1084+1del
ENST00000534319.5:c.814+1del
ENST00000534624.5:c.1522+1del
NM_006597.5:c.1522+1del
NM_153201.3:c.1387+136del NP_694881.1:n.1387+136del
XM_011542798.1:c.1522+1del
NM_006597.6:c.1522+1del
NM_153201.4:c.1387+136del NP_694881.1:n.1387+136del