Canonical Allele Identifier: CA2616532728

Gene: HSPA8

Linked Data

• gnomAD v4: 11-123058508-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058511_123058512del , CM000673.2:g.123058511_123058512del	GRCh38
NC_000011.9:g.122929219_122929220del , CM000673.1:g.122929219_122929220del	GRCh37
NC_000011.8:g.122434429_122434430del	NCBI36
NG_029473.1:g.8627_8628del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1523-26_1523-25del MANE Select	ENSP00000432083.1:n.1523-26_1523-25del
ENST00000227378.7:c.1523-26_1523-25del	ENSP00000227378.3:n.1523-26_1523-25del
ENST00000453788.6:c.1387+257_1387+258del	ENSP00000404372.2:n.1387+257_1387+258del
ENST00000524552.5:c.296-26_296-25del	ENSP00000435908.1:n.296-26_296-25del
ENST00000526110.5:c.1466-26_1466-25del	ENSP00000433584.1:n.1466-26_1466-25del
ENST00000526686.1:c.179-26_179-25del	ENSP00000435019.1:n.179-26_179-25del
ENST00000532091.1:n.1619_1620del
ENST00000532636.5:c.1523-26_1523-25del	ENSP00000437125.1:n.1523-26_1523-25del
ENST00000533540.5:c.1085-26_1085-25del	ENSP00000437189.1:n.1085-26_1085-25del
ENST00000534319.5:c.815-26_815-25del	ENSP00000433316.1:n.815-26_815-25del
ENST00000534624.5:c.1523-26_1523-25del	ENSP00000432083.1:n.1523-26_1523-25del
NM_006597.5:c.1523-26_1523-25del	NP_006588.1:n.1523-26_1523-25del
NM_153201.3:c.1387+257_1387+258del	NP_694881.1:n.1387+257_1387+258del
XM_011542798.1:c.1523-26_1523-25del	XP_011541100.1:n.1523-26_1523-25del
NM_006597.6:c.1523-26_1523-25del MANE Select	NP_006588.1:n.1523-26_1523-25del
NM_153201.4:c.1387+257_1387+258del	NP_694881.1:n.1387+257_1387+258del