Canonical Allele Identifier: CA383058152

Gene: HSPA8

Linked Data

• MyVariant Identifiers: chr11:g.122929834G>C (hg19) ; chr11:g.123059126G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059126G>C , CM000673.2:g.123059126G>C	GRCh38
NC_000011.9:g.122929834G>C , CM000673.1:g.122929834G>C	GRCh37
NC_000011.8:g.122435044G>C	NCBI36
NG_029473.1:g.8011C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1256C>G MANE Select	ENSP00000432083.1:p.Thr419Ser
ENST00000227378.7:c.1256C>G	ENSP00000227378.3:p.Thr419Ser
ENST00000453788.6:c.1256C>G	ENSP00000404372.2:p.Thr419Ser
ENST00000524552.5:c.29C>G	ENSP00000435908.1:p.Thr10Ser
ENST00000526110.5:c.1199C>G	ENSP00000433584.1:p.Thr400Ser
ENST00000532091.1:n.1003C>G
ENST00000532636.5:c.1256C>G	ENSP00000437125.1:p.Thr419Ser
ENST00000533238.5:n.381-23C>G
ENST00000533540.5:c.818C>G	ENSP00000437189.1:p.Thr273Ser
ENST00000534319.5:c.548C>G	ENSP00000433316.1:p.Thr183Ser
ENST00000534624.5:c.1256C>G	ENSP00000432083.1:p.Thr419Ser
NM_006597.5:c.1256C>G	NP_006588.1:p.Thr419Ser
NM_153201.3:c.1256C>G	NP_694881.1:p.Thr419Ser
XM_011542798.1:c.1256C>G	XP_011541100.1:p.Thr419Ser
NM_006597.6:c.1256C>G MANE Select	NP_006588.1:p.Thr419Ser
NM_153201.4:c.1256C>G	NP_694881.1:p.Thr419Ser