Canonical Allele Identifier: CA2616532721

Gene: HSPA8

Linked Data

• gnomAD v4: 11-123058466-T-TTTTAAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058466_123058467insTTTAAAG , CM000673.2:g.123058466_123058467insTTTAAAG	GRCh38
NC_000011.9:g.122929174_122929175insTTTAAAG , CM000673.1:g.122929174_122929175insTTTAAAG	GRCh37
NC_000011.8:g.122434384_122434385insTTTAAAG	NCBI36
NG_029473.1:g.8670_8671insCTTTAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1540_1541insCTTTAAA MANE Select	ENSP00000432083.1:p.Asp514AlafsTer5
ENST00000227378.7:c.1540_1541insCTTTAAA	ENSP00000227378.3:p.Asp514AlafsTer5
ENST00000453788.6:c.1387+300_1387+301insCTTTAAA	ENSP00000404372.2:n.1387+300_1387+301insCTTTAAA
ENST00000524552.5:c.313_314insCTTTAAA	ENSP00000435908.1:p.Asp105AlafsTer5
ENST00000526110.5:c.1483_1484insCTTTAAA	ENSP00000433584.1:p.Asp495AlafsTer5
ENST00000526686.1:c.196_197insCTTTAAA	ENSP00000435019.1:p.Asp66AlafsTer5
ENST00000532091.1:n.1662_1663insCTTTAAA
ENST00000532636.5:c.1540_1541insCTTTAAA	ENSP00000437125.1:p.Asp514AlafsTer5
ENST00000533540.5:c.1102_1103insCTTTAAA	ENSP00000437189.1:p.Asp368AlafsTer5
ENST00000534319.5:c.832_833insCTTTAAA	ENSP00000433316.1:p.Asp278AlafsTer5
ENST00000534624.5:c.1540_1541insCTTTAAA	ENSP00000432083.1:p.Asp514AlafsTer5
NM_006597.5:c.1540_1541insCTTTAAA	NP_006588.1:p.Asp514AlafsTer5
NM_153201.3:c.1387+300_1387+301insCTTTAAA	NP_694881.1:n.1387+300_1387+301insCTTTAAA
XM_011542798.1:c.1540_1541insCTTTAAA	XP_011541100.1:p.Asp514AlafsTer5
NM_006597.6:c.1540_1541insCTTTAAA MANE Select	NP_006588.1:p.Asp514AlafsTer5
NM_153201.4:c.1387+300_1387+301insCTTTAAA	NP_694881.1:n.1387+300_1387+301insCTTTAAA