Canonical Allele Identifier: CA477385242

Gene: HSPA8

Linked Data

• MyVariant Identifiers: chr11:g.122929158G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058450G>A , CM000673.2:g.123058450G>A	GRCh38
NC_000011.9:g.122929158G>A , CM000673.1:g.122929158G>A	GRCh37
NC_000011.8:g.122434368G>A	NCBI36
NG_029473.1:g.8687C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1557C>T MANE Select	ENSP00000432083.1:p.Val519=
ENST00000227378.7:c.1557C>T	ENSP00000227378.3:p.Val519=
ENST00000453788.6:c.1387+317C>T	ENSP00000404372.2:n.1387+317C>T
ENST00000524552.5:c.330C>T	ENSP00000435908.1:p.Val110=
ENST00000526110.5:c.1500C>T	ENSP00000433584.1:p.Val500=
ENST00000526686.1:c.213C>T	ENSP00000435019.1:p.Val71=
ENST00000532091.1:n.1679C>T
ENST00000532636.5:c.1557C>T	ENSP00000437125.1:p.Val519=
ENST00000533540.5:c.1119C>T	ENSP00000437189.1:p.Val373=
ENST00000534319.5:c.849C>T	ENSP00000433316.1:p.Val283=
ENST00000534624.5:c.1557C>T	ENSP00000432083.1:p.Val519=
NM_006597.5:c.1557C>T	NP_006588.1:p.Val519=
NM_153201.3:c.1387+317C>T	NP_694881.1:n.1387+317C>T
XM_011542798.1:c.1557C>T	XP_011541100.1:p.Val519=
NM_006597.6:c.1557C>T MANE Select	NP_006588.1:p.Val519=
NM_153201.4:c.1387+317C>T	NP_694881.1:n.1387+317C>T