Canonical Allele Identifier: CA383057463

Gene: HSPA8

Linked Data

• MyVariant Identifiers: chr11:g.122929525T>A (hg19) ; chr11:g.123058817T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058817T>A , CM000673.2:g.123058817T>A	GRCh38
NC_000011.9:g.122929525T>A , CM000673.1:g.122929525T>A	GRCh37
NC_000011.8:g.122434735T>A	NCBI36
NG_029473.1:g.8320A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000534624.6:c.1337A>T MANE Select	ENSP00000432083.1:p.Glu446Val
ENST00000227378.7:c.1337A>T	ENSP00000227378.3:p.Glu446Val
ENST00000453788.6:c.1337A>T	ENSP00000404372.2:p.Glu446Val
ENST00000524552.5:c.110A>T	ENSP00000435908.1:p.Glu37Val
ENST00000526110.5:c.1280A>T	ENSP00000433584.1:p.Glu427Val
ENST00000526686.1:c.-8A>T	ENSP00000435019.1:n.-8A>T
ENST00000532091.1:n.1312A>T
ENST00000532636.5:c.1337A>T	ENSP00000437125.1:p.Glu446Val
ENST00000533238.5:n.439A>T
ENST00000533540.5:c.899A>T	ENSP00000437189.1:p.Glu300Val
ENST00000534319.5:c.629A>T	ENSP00000433316.1:p.Glu210Val
ENST00000534624.5:c.1337A>T	ENSP00000432083.1:p.Glu446Val
NM_006597.5:c.1337A>T	NP_006588.1:p.Glu446Val
NM_153201.3:c.1337A>T	NP_694881.1:p.Glu446Val
XM_011542798.1:c.1337A>T	XP_011541100.1:p.Glu446Val
NM_006597.6:c.1337A>T MANE Select	NP_006588.1:p.Glu446Val
NM_153201.4:c.1337A>T	NP_694881.1:p.Glu446Val