Canonical Allele Identifier: CA2616532895

Gene: HSPA8

Linked Data

• gnomAD v4: 11-123059274-AAGTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059276_123059279del , CM000673.2:g.123059276_123059279del	GRCh38
NC_000011.9:g.122929984_122929987del , CM000673.1:g.122929984_122929987del	GRCh37
NC_000011.8:g.122435194_122435197del	NCBI36
NG_029473.1:g.7859_7862del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1121-17_1121-14del MANE Select	ENSP00000432083.1:n.1121-17_1121-14del
ENST00000227378.7:c.1121-17_1121-14del	ENSP00000227378.3:n.1121-17_1121-14del
ENST00000453788.6:c.1121-17_1121-14del	ENSP00000404372.2:n.1121-17_1121-14del
ENST00000524552.5:c.-124_-121del	ENSP00000435908.1:n.-124_-121del
ENST00000526110.5:c.1064-17_1064-14del	ENSP00000433584.1:n.1064-17_1064-14del
ENST00000526862.1:n.399-17_399-14del
ENST00000527983.5:n.1464_1467del
ENST00000532091.1:n.868-17_868-14del
ENST00000532636.5:c.1121-17_1121-14del	ENSP00000437125.1:n.1121-17_1121-14del
ENST00000533238.5:n.381-175_381-172del
ENST00000533540.5:c.683-17_683-14del	ENSP00000437189.1:n.683-17_683-14del
ENST00000534319.5:c.413-17_413-14del	ENSP00000433316.1:n.413-17_413-14del
ENST00000534624.5:c.1121-17_1121-14del	ENSP00000432083.1:n.1121-17_1121-14del
NM_006597.5:c.1121-17_1121-14del	NP_006588.1:n.1121-17_1121-14del
NM_153201.3:c.1121-17_1121-14del	NP_694881.1:n.1121-17_1121-14del
XM_011542798.1:c.1121-17_1121-14del	XP_011541100.1:n.1121-17_1121-14del
NM_006597.6:c.1121-17_1121-14del MANE Select	NP_006588.1:n.1121-17_1121-14del
NM_153201.4:c.1121-17_1121-14del	NP_694881.1:n.1121-17_1121-14del