Canonical Allele Identifier: CA229966670

Gene: HSPA8

Linked Data

• dbSNP Id: rs370356082
• gnomAD v3: 11-123058551-TTAGC-T
• gnomAD v4: 11-123058551-TTAGC-T
• MyVariant Identifiers: chr11:g.122929260_122929263del (hg19) ; chr11:g.123058552_123058555del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058555_123058558del , CM000673.2:g.123058555_123058558del	GRCh38
NC_000011.9:g.122929263_122929266del , CM000673.1:g.122929263_122929266del	GRCh37
NC_000011.8:g.122434473_122434476del	NCBI36
NG_029473.1:g.8582_8585del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1523-71_1523-68del MANE Select	ENSP00000432083.1:n.1523-71_1523-68del
ENST00000227378.7:c.1523-71_1523-68del	ENSP00000227378.3:n.1523-71_1523-68del
ENST00000453788.6:c.1387+212_1387+215del	ENSP00000404372.2:n.1387+212_1387+215del
ENST00000524552.5:c.296-71_296-68del	ENSP00000435908.1:n.296-71_296-68del
ENST00000526110.5:c.1466-71_1466-68del	ENSP00000433584.1:n.1466-71_1466-68del
ENST00000526686.1:c.179-71_179-68del	ENSP00000435019.1:n.179-71_179-68del
ENST00000532091.1:n.1574_1577del
ENST00000532636.5:c.1523-71_1523-68del	ENSP00000437125.1:n.1523-71_1523-68del
ENST00000533540.5:c.1085-71_1085-68del	ENSP00000437189.1:n.1085-71_1085-68del
ENST00000534319.5:c.815-71_815-68del	ENSP00000433316.1:n.815-71_815-68del
ENST00000534624.5:c.1523-71_1523-68del	ENSP00000432083.1:n.1523-71_1523-68del
NM_006597.5:c.1523-71_1523-68del	NP_006588.1:n.1523-71_1523-68del
NM_153201.3:c.1387+212_1387+215del	NP_694881.1:n.1387+212_1387+215del
XM_011542798.1:c.1523-71_1523-68del	XP_011541100.1:n.1523-71_1523-68del
NM_006597.6:c.1523-71_1523-68del MANE Select	NP_006588.1:n.1523-71_1523-68del
NM_153201.4:c.1387+212_1387+215del	NP_694881.1:n.1387+212_1387+215del