Canonical Allele Identifier: CA2616532739

Gene: HSPA8

Linked Data

• gnomAD v4: 11-123058535-G-GTGTAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058536_123058537insGTAAAT , CM000673.2:g.123058536_123058537insGTAAAT	GRCh38
NC_000011.9:g.122929244_122929245insGTAAAT , CM000673.1:g.122929244_122929245insGTAAAT	GRCh37
NC_000011.8:g.122434454_122434455insGTAAAT	NCBI36
NG_029473.1:g.8601_8602insTTTACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1523-52_1523-51insTTTACA MANE Select	ENSP00000432083.1:n.1523-52_1523-51insTTTACA
ENST00000227378.7:c.1523-52_1523-51insTTTACA	ENSP00000227378.3:n.1523-52_1523-51insTTTACA
ENST00000453788.6:c.1387+231_1387+232insTTTACA	ENSP00000404372.2:n.1387+231_1387+232insTTTACA
ENST00000524552.5:c.296-52_296-51insTTTACA	ENSP00000435908.1:n.296-52_296-51insTTTACA
ENST00000526110.5:c.1466-52_1466-51insTTTACA	ENSP00000433584.1:n.1466-52_1466-51insTTTACA
ENST00000526686.1:c.179-52_179-51insTTTACA	ENSP00000435019.1:n.179-52_179-51insTTTACA
ENST00000532091.1:n.1593_1594insTTTACA
ENST00000532636.5:c.1523-52_1523-51insTTTACA	ENSP00000437125.1:n.1523-52_1523-51insTTTACA
ENST00000533540.5:c.1085-52_1085-51insTTTACA	ENSP00000437189.1:n.1085-52_1085-51insTTTACA
ENST00000534319.5:c.815-52_815-51insTTTACA	ENSP00000433316.1:n.815-52_815-51insTTTACA
ENST00000534624.5:c.1523-52_1523-51insTTTACA	ENSP00000432083.1:n.1523-52_1523-51insTTTACA
NM_006597.5:c.1523-52_1523-51insTTTACA	NP_006588.1:n.1523-52_1523-51insTTTACA
NM_153201.3:c.1387+231_1387+232insTTTACA	NP_694881.1:n.1387+231_1387+232insTTTACA
XM_011542798.1:c.1523-52_1523-51insTTTACA	XP_011541100.1:n.1523-52_1523-51insTTTACA
NM_006597.6:c.1523-52_1523-51insTTTACA MANE Select	NP_006588.1:n.1523-52_1523-51insTTTACA
NM_153201.4:c.1387+231_1387+232insTTTACA	NP_694881.1:n.1387+231_1387+232insTTTACA