Canonical Allele Identifier: CA2005595759

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058847_123058848delinsAC , CM000673.2:g.123058847_123058848delinsAC	GRCh38
NC_000011.9:g.122929555_122929556delinsAC , CM000673.1:g.122929555_122929556delinsAC	GRCh37
NC_000011.8:g.122434765_122434766delinsAC	NCBI36
NG_029473.1:g.8289_8290delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1324-18_1324-17delinsGT MANE Select	ENSP00000432083.1:n.1324-18_1324-17delinsGT
ENST00000227378.7:c.1324-18_1324-17delinsGT	ENSP00000227378.3:n.1324-18_1324-17delinsGT
ENST00000453788.6:c.1324-18_1324-17delinsGT	ENSP00000404372.2:n.1324-18_1324-17delinsGT
ENST00000524552.5:c.97-18_97-17delinsGT	ENSP00000435908.1:n.97-18_97-17delinsGT
ENST00000526110.5:c.1267-18_1267-17delinsGT	ENSP00000433584.1:n.1267-18_1267-17delinsGT
ENST00000526686.1:c.-39_-38delinsGT	ENSP00000435019.1:n.-39_-38delinsGT
ENST00000532091.1:n.1281_1282delinsGT
ENST00000532636.5:c.1324-18_1324-17delinsGT	ENSP00000437125.1:n.1324-18_1324-17delinsGT
ENST00000533238.5:n.426-18_426-17delinsGT
ENST00000533540.5:c.886-18_886-17delinsGT	ENSP00000437189.1:n.886-18_886-17delinsGT
ENST00000534319.5:c.616-18_616-17delinsGT	ENSP00000433316.1:n.616-18_616-17delinsGT
ENST00000534624.5:c.1324-18_1324-17delinsGT	ENSP00000432083.1:n.1324-18_1324-17delinsGT
NM_006597.5:c.1324-18_1324-17delinsGT	NP_006588.1:n.1324-18_1324-17delinsGT
NM_153201.3:c.1324-18_1324-17delinsGT	NP_694881.1:n.1324-18_1324-17delinsGT
XM_011542798.1:c.1324-18_1324-17delinsGT	XP_011541100.1:n.1324-18_1324-17delinsGT
NM_006597.6:c.1324-18_1324-17delinsGT MANE Select	NP_006588.1:n.1324-18_1324-17delinsGT
NM_153201.4:c.1324-18_1324-17delinsGT	NP_694881.1:n.1324-18_1324-17delinsGT