Canonical Allele Identifier: CA943027659

Gene: HSPA8

Linked Data

• dbSNP Id: rs1865385841
• gnomAD v3: 11-123058500-ACTC-A
• gnomAD v4: 11-123058500-ACTC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058501_123058503del , CM000673.2:g.123058501_123058503del	GRCh38
NC_000011.9:g.122929209_122929211del , CM000673.1:g.122929209_122929211del	GRCh37
NC_000011.8:g.122434419_122434421del	NCBI36
NG_029473.1:g.8634_8636del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1523-19_1523-17del MANE Select	ENSP00000432083.1:n.1523-19_1523-17del
ENST00000227378.7:c.1523-19_1523-17del	ENSP00000227378.3:n.1523-19_1523-17del
ENST00000453788.6:c.1387+264_1387+266del	ENSP00000404372.2:n.1387+264_1387+266del
ENST00000524552.5:c.296-19_296-17del	ENSP00000435908.1:n.296-19_296-17del
ENST00000526110.5:c.1466-19_1466-17del	ENSP00000433584.1:n.1466-19_1466-17del
ENST00000526686.1:c.179-19_179-17del	ENSP00000435019.1:n.179-19_179-17del
ENST00000532091.1:n.1626_1628del
ENST00000532636.5:c.1523-19_1523-17del	ENSP00000437125.1:n.1523-19_1523-17del
ENST00000533540.5:c.1085-19_1085-17del	ENSP00000437189.1:n.1085-19_1085-17del
ENST00000534319.5:c.815-19_815-17del	ENSP00000433316.1:n.815-19_815-17del
ENST00000534624.5:c.1523-19_1523-17del	ENSP00000432083.1:n.1523-19_1523-17del
NM_006597.5:c.1523-19_1523-17del	NP_006588.1:n.1523-19_1523-17del
NM_153201.3:c.1387+264_1387+266del	NP_694881.1:n.1387+264_1387+266del
XM_011542798.1:c.1523-19_1523-17del	XP_011541100.1:n.1523-19_1523-17del
NM_006597.6:c.1523-19_1523-17del MANE Select	NP_006588.1:n.1523-19_1523-17del
NM_153201.4:c.1387+264_1387+266del	NP_694881.1:n.1387+264_1387+266del