Canonical Allele Identifier: CA2005594877

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058503_123058507delinsCTAAG , CM000673.2:g.123058503_123058507delinsCTAAG	GRCh38
NC_000011.9:g.122929211_122929215delinsCTAAG , CM000673.1:g.122929211_122929215delinsCTAAG	GRCh37
NC_000011.8:g.122434421_122434425delinsCTAAG	NCBI36
NG_029473.1:g.8630_8634delinsCTTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1523-23_1523-19delinsCTTAG MANE Select	ENSP00000432083.1:n.1523-23_1523-19delinsCTTAG
ENST00000227378.7:c.1523-23_1523-19delinsCTTAG	ENSP00000227378.3:n.1523-23_1523-19delinsCTTAG
ENST00000453788.6:c.1387+260_1387+264delinsCTTAG	ENSP00000404372.2:n.1387+260_1387+264delinsCTTAG
ENST00000524552.5:c.296-23_296-19delinsCTTAG	ENSP00000435908.1:n.296-23_296-19delinsCTTAG
ENST00000526110.5:c.1466-23_1466-19delinsCTTAG	ENSP00000433584.1:n.1466-23_1466-19delinsCTTAG
ENST00000526686.1:c.179-23_179-19delinsCTTAG	ENSP00000435019.1:n.179-23_179-19delinsCTTAG
ENST00000532091.1:n.1622_1626delinsCTTAG
ENST00000532636.5:c.1523-23_1523-19delinsCTTAG	ENSP00000437125.1:n.1523-23_1523-19delinsCTTAG
ENST00000533540.5:c.1085-23_1085-19delinsCTTAG	ENSP00000437189.1:n.1085-23_1085-19delinsCTTAG
ENST00000534319.5:c.815-23_815-19delinsCTTAG	ENSP00000433316.1:n.815-23_815-19delinsCTTAG
ENST00000534624.5:c.1523-23_1523-19delinsCTTAG	ENSP00000432083.1:n.1523-23_1523-19delinsCTTAG
NM_006597.5:c.1523-23_1523-19delinsCTTAG	NP_006588.1:n.1523-23_1523-19delinsCTTAG
NM_153201.3:c.1387+260_1387+264delinsCTTAG	NP_694881.1:n.1387+260_1387+264delinsCTTAG
XM_011542798.1:c.1523-23_1523-19delinsCTTAG	XP_011541100.1:n.1523-23_1523-19delinsCTTAG
NM_006597.6:c.1523-23_1523-19delinsCTTAG MANE Select	NP_006588.1:n.1523-23_1523-19delinsCTTAG
NM_153201.4:c.1387+260_1387+264delinsCTTAG	NP_694881.1:n.1387+260_1387+264delinsCTTAG