Canonical Allele Identifier: CA2005594818

Gene: HSPA8

Linked Data

• dbSNP Id: rs1591436089

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058495A>C , CM000673.2:g.123058495A>C	GRCh38
NC_000011.9:g.122929203A>C , CM000673.1:g.122929203A>C	GRCh37
NC_000011.8:g.122434413A>C	NCBI36
NG_029473.1:g.8642T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1523-11T>G MANE Select	ENSP00000432083.1:n.1523-11T>G
ENST00000227378.7:c.1523-11T>G	ENSP00000227378.3:n.1523-11T>G
ENST00000453788.6:c.1387+272T>G	ENSP00000404372.2:n.1387+272T>G
ENST00000524552.5:c.296-11T>G	ENSP00000435908.1:n.296-11T>G
ENST00000526110.5:c.1466-11T>G	ENSP00000433584.1:n.1466-11T>G
ENST00000526686.1:c.179-11T>G	ENSP00000435019.1:n.179-11T>G
ENST00000532091.1:n.1634T>G
ENST00000532636.5:c.1523-11T>G	ENSP00000437125.1:n.1523-11T>G
ENST00000533540.5:c.1085-11T>G	ENSP00000437189.1:n.1085-11T>G
ENST00000534319.5:c.815-11T>G	ENSP00000433316.1:n.815-11T>G
ENST00000534624.5:c.1523-11T>G	ENSP00000432083.1:n.1523-11T>G
NM_006597.5:c.1523-11T>G	NP_006588.1:n.1523-11T>G
NM_153201.3:c.1387+272T>G	NP_694881.1:n.1387+272T>G
XM_011542798.1:c.1523-11T>G	XP_011541100.1:n.1523-11T>G
NM_006597.6:c.1523-11T>G MANE Select	NP_006588.1:n.1523-11T>G
NM_153201.4:c.1387+272T>G	NP_694881.1:n.1387+272T>G