Canonical Allele Identifier: CA2616532754

Gene: HSPA8

Linked Data

• gnomAD v4: 11-123058553-AGCTAGACGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058554_123058562del , CM000673.2:g.123058554_123058562del	GRCh38
NC_000011.9:g.122929262_122929270del , CM000673.1:g.122929262_122929270del	GRCh37
NC_000011.8:g.122434472_122434480del	NCBI36
NG_029473.1:g.8575_8583del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1522+70_1523-70del MANE Select	ENSP00000432083.1:n.1522+70_1523-70del
ENST00000227378.7:c.1522+70_1523-70del	ENSP00000227378.3:n.1522+70_1523-70del
ENST00000453788.6:c.1387+205_1387+213del	ENSP00000404372.2:n.1387+205_1387+213del
ENST00000524552.5:c.295+70_296-70del	ENSP00000435908.1:n.295+70_296-70del
ENST00000526110.5:c.1465+70_1466-70del	ENSP00000433584.1:n.1465+70_1466-70del
ENST00000526686.1:c.178+70_179-70del	ENSP00000435019.1:n.178+70_179-70del
ENST00000532091.1:n.1567_1575del
ENST00000532636.5:c.1522+70_1523-70del	ENSP00000437125.1:n.1522+70_1523-70del
ENST00000533540.5:c.1084+70_1085-70del	ENSP00000437189.1:n.1084+70_1085-70del
ENST00000534319.5:c.814+70_815-70del	ENSP00000433316.1:n.814+70_815-70del
ENST00000534624.5:c.1522+70_1523-70del	ENSP00000432083.1:n.1522+70_1523-70del
NM_006597.5:c.1522+70_1523-70del	NP_006588.1:n.1522+70_1523-70del
NM_153201.3:c.1387+205_1387+213del	NP_694881.1:n.1387+205_1387+213del
XM_011542798.1:c.1522+70_1523-70del	XP_011541100.1:n.1522+70_1523-70del
NM_006597.6:c.1522+70_1523-70del MANE Select	NP_006588.1:n.1522+70_1523-70del
NM_153201.4:c.1387+205_1387+213del	NP_694881.1:n.1387+205_1387+213del