Canonical Allele Identifier: CA2616532798

Gene: HSPA8

Linked Data

• gnomAD v4: 11-123058832-T-TGAATAAGCACACCAGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058832_123058833insGAATAAGCACACCAGGC , CM000673.2:g.123058832_123058833insGAATAAGCACACCAGGC	GRCh38
NC_000011.9:g.122929540_122929541insGAATAAGCACACCAGGC , CM000673.1:g.122929540_122929541insGAATAAGCACACCAGGC	GRCh37
NC_000011.8:g.122434750_122434751insGAATAAGCACACCAGGC	NCBI36
NG_029473.1:g.8304_8305insGCCTGGTGTGCTTATTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1324-3_1324-2insGCCTGGTGTGCTTATTC MANE Select	ENSP00000432083.1:n.1324-3_1324-2insGCCTGGTGTGCTTATTC
ENST00000227378.7:c.1324-3_1324-2insGCCTGGTGTGCTTATTC	ENSP00000227378.3:n.1324-3_1324-2insGCCTGGTGTGCTTATTC
ENST00000453788.6:c.1324-3_1324-2insGCCTGGTGTGCTTATTC	ENSP00000404372.2:n.1324-3_1324-2insGCCTGGTGTGCTTATTC
ENST00000524552.5:c.97-3_97-2insGCCTGGTGTGCTTATTC	ENSP00000435908.1:n.97-3_97-2insGCCTGGTGTGCTTATTC
ENST00000526110.5:c.1267-3_1267-2insGCCTGGTGTGCTTATTC	ENSP00000433584.1:n.1267-3_1267-2insGCCTGGTGTGCTTATTC
ENST00000526686.1:c.-24_-23insGCCTGGTGTGCTTATTC	ENSP00000435019.1:n.-24_-23insGCCTGGTGTGCTTATTC
ENST00000532091.1:n.1296_1297insGCCTGGTGTGCTTATTC
ENST00000532636.5:c.1324-3_1324-2insGCCTGGTGTGCTTATTC	ENSP00000437125.1:n.1324-3_1324-2insGCCTGGTGTGCTTATTC
ENST00000533238.5:n.426-3_426-2insGCCTGGTGTGCTTATTC
ENST00000533540.5:c.886-3_886-2insGCCTGGTGTGCTTATTC	ENSP00000437189.1:n.886-3_886-2insGCCTGGTGTGCTTATTC
ENST00000534319.5:c.616-3_616-2insGCCTGGTGTGCTTATTC	ENSP00000433316.1:n.616-3_616-2insGCCTGGTGTGCTTATTC
ENST00000534624.5:c.1324-3_1324-2insGCCTGGTGTGCTTATTC	ENSP00000432083.1:n.1324-3_1324-2insGCCTGGTGTGCTTATTC
NM_006597.5:c.1324-3_1324-2insGCCTGGTGTGCTTATTC	NP_006588.1:n.1324-3_1324-2insGCCTGGTGTGCTTATTC
NM_153201.3:c.1324-3_1324-2insGCCTGGTGTGCTTATTC	NP_694881.1:n.1324-3_1324-2insGCCTGGTGTGCTTATTC
XM_011542798.1:c.1324-3_1324-2insGCCTGGTGTGCTTATTC	XP_011541100.1:n.1324-3_1324-2insGCCTGGTGTGCTTATTC
NM_006597.6:c.1324-3_1324-2insGCCTGGTGTGCTTATTC MANE Select	NP_006588.1:n.1324-3_1324-2insGCCTGGTGTGCTTATTC
NM_153201.4:c.1324-3_1324-2insGCCTGGTGTGCTTATTC	NP_694881.1:n.1324-3_1324-2insGCCTGGTGTGCTTATTC