Canonical Allele Identifier: CA383056878

Gene: HSPA8

Linked Data

• MyVariant Identifiers: chr11:g.122929154C>A (hg19) ; chr11:g.123058446C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058446C>A , CM000673.2:g.123058446C>A	GRCh38
NC_000011.9:g.122929154C>A , CM000673.1:g.122929154C>A	GRCh37
NC_000011.8:g.122434364C>A	NCBI36
NG_029473.1:g.8691G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1561G>T MANE Select	ENSP00000432083.1:p.Glu521Ter
ENST00000227378.7:c.1561G>T	ENSP00000227378.3:p.Glu521Ter
ENST00000453788.6:c.1387+321G>T	ENSP00000404372.2:n.1387+321G>T
ENST00000524552.5:c.334G>T	ENSP00000435908.1:p.Glu112Ter
ENST00000526110.5:c.1504G>T	ENSP00000433584.1:p.Glu502Ter
ENST00000526686.1:c.217G>T	ENSP00000435019.1:p.Glu73Ter
ENST00000532091.1:n.1683G>T
ENST00000532636.5:c.1561G>T	ENSP00000437125.1:p.Glu521Ter
ENST00000533540.5:c.1123G>T	ENSP00000437189.1:p.Glu375Ter
ENST00000534319.5:c.853G>T	ENSP00000433316.1:p.Glu285Ter
ENST00000534624.5:c.1561G>T	ENSP00000432083.1:p.Glu521Ter
NM_006597.5:c.1561G>T	NP_006588.1:p.Glu521Ter
NM_153201.3:c.1387+321G>T	NP_694881.1:n.1387+321G>T
XM_011542798.1:c.1561G>T	XP_011541100.1:p.Glu521Ter
NM_006597.6:c.1561G>T MANE Select	NP_006588.1:p.Glu521Ter
NM_153201.4:c.1387+321G>T	NP_694881.1:n.1387+321G>T