Canonical Allele Identifier: CA2005595919

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058891_123058894delinsCCTG , CM000673.2:g.123058891_123058894delinsCCTG	GRCh38
NC_000011.9:g.122929599_122929602delinsCCTG , CM000673.1:g.122929599_122929602delinsCCTG	GRCh37
NC_000011.8:g.122434809_122434812delinsCCTG	NCBI36
NG_029473.1:g.8243_8246delinsCAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1324-64_1324-61delinsCAGG MANE Select	ENSP00000432083.1:n.1324-64_1324-61delinsCAGG
ENST00000227378.7:c.1324-64_1324-61delinsCAGG	ENSP00000227378.3:n.1324-64_1324-61delinsCAGG
ENST00000453788.6:c.1324-64_1324-61delinsCAGG	ENSP00000404372.2:n.1324-64_1324-61delinsCAGG
ENST00000524552.5:c.97-64_97-61delinsCAGG	ENSP00000435908.1:n.97-64_97-61delinsCAGG
ENST00000526110.5:c.1267-64_1267-61delinsCAGG	ENSP00000433584.1:n.1267-64_1267-61delinsCAGG
ENST00000526686.1:c.-85_-82delinsCAGG	ENSP00000435019.1:n.-85_-82delinsCAGG
ENST00000532091.1:n.1235_1238delinsCAGG
ENST00000532636.5:c.1324-64_1324-61delinsCAGG	ENSP00000437125.1:n.1324-64_1324-61delinsCAGG
ENST00000533238.5:n.426-64_426-61delinsCAGG
ENST00000533540.5:c.886-64_886-61delinsCAGG	ENSP00000437189.1:n.886-64_886-61delinsCAGG
ENST00000534319.5:c.616-64_616-61delinsCAGG	ENSP00000433316.1:n.616-64_616-61delinsCAGG
ENST00000534624.5:c.1324-64_1324-61delinsCAGG	ENSP00000432083.1:n.1324-64_1324-61delinsCAGG
NM_006597.5:c.1324-64_1324-61delinsCAGG	NP_006588.1:n.1324-64_1324-61delinsCAGG
NM_153201.3:c.1324-64_1324-61delinsCAGG	NP_694881.1:n.1324-64_1324-61delinsCAGG
XM_011542798.1:c.1324-64_1324-61delinsCAGG	XP_011541100.1:n.1324-64_1324-61delinsCAGG
NM_006597.6:c.1324-64_1324-61delinsCAGG MANE Select	NP_006588.1:n.1324-64_1324-61delinsCAGG
NM_153201.4:c.1324-64_1324-61delinsCAGG	NP_694881.1:n.1324-64_1324-61delinsCAGG