Canonical Allele Identifier: CA383056858

Gene: HSPA8

Linked Data

• MyVariant Identifiers: chr11:g.122929145T>A (hg19) ; chr11:g.123058437T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058437T>A , CM000673.2:g.123058437T>A	GRCh38
NC_000011.9:g.122929145T>A , CM000673.1:g.122929145T>A	GRCh37
NC_000011.8:g.122434355T>A	NCBI36
NG_029473.1:g.8700A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1570A>T MANE Select	ENSP00000432083.1:p.Lys524Ter
ENST00000227378.7:c.1570A>T	ENSP00000227378.3:p.Lys524Ter
ENST00000453788.6:c.1387+330A>T	ENSP00000404372.2:n.1387+330A>T
ENST00000524552.5:c.343A>T	ENSP00000435908.1:p.Lys115Ter
ENST00000526110.5:c.1513A>T	ENSP00000433584.1:p.Lys505Ter
ENST00000526686.1:c.226A>T	ENSP00000435019.1:p.Lys76Ter
ENST00000532091.1:n.1692A>T
ENST00000532636.5:c.1570A>T	ENSP00000437125.1:p.Lys524Ter
ENST00000533540.5:c.1132A>T	ENSP00000437189.1:p.Lys378Ter
ENST00000534319.5:c.862A>T	ENSP00000433316.1:p.Lys288Ter
ENST00000534624.5:c.1570A>T	ENSP00000432083.1:p.Lys524Ter
NM_006597.5:c.1570A>T	NP_006588.1:p.Lys524Ter
NM_153201.3:c.1387+330A>T	NP_694881.1:n.1387+330A>T
XM_011542798.1:c.1570A>T	XP_011541100.1:p.Lys524Ter
NM_006597.6:c.1570A>T MANE Select	NP_006588.1:p.Lys524Ter
NM_153201.4:c.1387+330A>T	NP_694881.1:n.1387+330A>T