Canonical Allele Identifier: CA383056968

Gene: HSPA8

Linked Data

• MyVariant Identifiers: chr11:g.122929192C>T (hg19) ; chr11:g.123058484C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058484C>T , CM000673.2:g.123058484C>T	GRCh38
NC_000011.9:g.122929192C>T , CM000673.1:g.122929192C>T	GRCh37
NC_000011.8:g.122434402C>T	NCBI36
NG_029473.1:g.8653G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1523G>A MANE Select	ENSP00000432083.1:p.Gly508Asp
ENST00000227378.7:c.1523G>A	ENSP00000227378.3:p.Gly508Asp
ENST00000453788.6:c.1387+283G>A	ENSP00000404372.2:n.1387+283G>A
ENST00000524552.5:c.296G>A	ENSP00000435908.1:p.Gly99Asp
ENST00000526110.5:c.1466G>A	ENSP00000433584.1:p.Gly489Asp
ENST00000526686.1:c.179G>A	ENSP00000435019.1:p.Gly60Asp
ENST00000532091.1:n.1645G>A
ENST00000532636.5:c.1523G>A	ENSP00000437125.1:p.Gly508Asp
ENST00000533540.5:c.1085G>A	ENSP00000437189.1:p.Gly362Asp
ENST00000534319.5:c.815G>A	ENSP00000433316.1:p.Gly272Asp
ENST00000534624.5:c.1523G>A	ENSP00000432083.1:p.Gly508Asp
NM_006597.5:c.1523G>A	NP_006588.1:p.Gly508Asp
NM_153201.3:c.1387+283G>A	NP_694881.1:n.1387+283G>A
XM_011542798.1:c.1523G>A	XP_011541100.1:p.Gly508Asp
NM_006597.6:c.1523G>A MANE Select	NP_006588.1:p.Gly508Asp
NM_153201.4:c.1387+283G>A	NP_694881.1:n.1387+283G>A