Canonical Allele Identifier: CA383056981

Gene: HSPA8

Linked Data

• MyVariant Identifiers: chr11:g.122929340C>A (hg19) ; chr11:g.123058632C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058632C>A , CM000673.2:g.123058632C>A	GRCh38
NC_000011.9:g.122929340C>A , CM000673.1:g.122929340C>A	GRCh37
NC_000011.8:g.122434550C>A	NCBI36
NG_029473.1:g.8505G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1522G>T MANE Select	ENSP00000432083.1:p.Gly508Cys
ENST00000227378.7:c.1522G>T	ENSP00000227378.3:p.Gly508Cys
ENST00000453788.6:c.1387+135G>T	ENSP00000404372.2:n.1387+135G>T
ENST00000524552.5:c.295G>T	ENSP00000435908.1:p.Gly99Cys
ENST00000526110.5:c.1465G>T	ENSP00000433584.1:p.Gly489Cys
ENST00000526686.1:c.178G>T	ENSP00000435019.1:p.Gly60Cys
ENST00000532091.1:n.1497G>T
ENST00000532636.5:c.1522G>T	ENSP00000437125.1:p.Gly508Cys
ENST00000533540.5:c.1084G>T	ENSP00000437189.1:p.Gly362Cys
ENST00000534319.5:c.814G>T	ENSP00000433316.1:p.Gly272Cys
ENST00000534624.5:c.1522G>T	ENSP00000432083.1:p.Gly508Cys
NM_006597.5:c.1522G>T	NP_006588.1:p.Gly508Cys
NM_153201.3:c.1387+135G>T	NP_694881.1:n.1387+135G>T
XM_011542798.1:c.1522G>T	XP_011541100.1:p.Gly508Cys
NM_006597.6:c.1522G>T MANE Select	NP_006588.1:p.Gly508Cys
NM_153201.4:c.1387+135G>T	NP_694881.1:n.1387+135G>T