Canonical Allele Identifier: CA672748443

Gene: HSPA8

Linked Data

• dbSNP Id: rs1301434880
• MyVariant Identifiers: chr11:g.122929212_122929215del (hg19) ; chr11:g.123058504_123058507del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058507_123058510del , CM000673.2:g.123058507_123058510del	GRCh38
NC_000011.9:g.122929215_122929218del , CM000673.1:g.122929215_122929218del	GRCh37
NC_000011.8:g.122434425_122434428del	NCBI36
NG_029473.1:g.8630_8633del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1523-23_1523-20del MANE Select	ENSP00000432083.1:n.1523-23_1523-20del
ENST00000227378.7:c.1523-23_1523-20del	ENSP00000227378.3:n.1523-23_1523-20del
ENST00000453788.6:c.1387+260_1387+263del	ENSP00000404372.2:n.1387+260_1387+263del
ENST00000524552.5:c.296-23_296-20del	ENSP00000435908.1:n.296-23_296-20del
ENST00000526110.5:c.1466-23_1466-20del	ENSP00000433584.1:n.1466-23_1466-20del
ENST00000526686.1:c.179-23_179-20del	ENSP00000435019.1:n.179-23_179-20del
ENST00000532091.1:n.1622_1625del
ENST00000532636.5:c.1523-23_1523-20del	ENSP00000437125.1:n.1523-23_1523-20del
ENST00000533540.5:c.1085-23_1085-20del	ENSP00000437189.1:n.1085-23_1085-20del
ENST00000534319.5:c.815-23_815-20del	ENSP00000433316.1:n.815-23_815-20del
ENST00000534624.5:c.1523-23_1523-20del	ENSP00000432083.1:n.1523-23_1523-20del
NM_006597.5:c.1523-23_1523-20del	NP_006588.1:n.1523-23_1523-20del
NM_153201.3:c.1387+260_1387+263del	NP_694881.1:n.1387+260_1387+263del
XM_011542798.1:c.1523-23_1523-20del	XP_011541100.1:n.1523-23_1523-20del
NM_006597.6:c.1523-23_1523-20del MANE Select	NP_006588.1:n.1523-23_1523-20del
NM_153201.4:c.1387+260_1387+263del	NP_694881.1:n.1387+260_1387+263del