Canonical Allele Identifier: CA477385372

Gene: HSPA8

Linked Data

• MyVariant Identifiers: chr11:g.122929497C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058789C>A , CM000673.2:g.123058789C>A	GRCh38
NC_000011.9:g.122929497C>A , CM000673.1:g.122929497C>A	GRCh37
NC_000011.8:g.122434707C>A	NCBI36
NG_029473.1:g.8348G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1365G>T MANE Select	ENSP00000432083.1:p.Leu455=
ENST00000227378.7:c.1365G>T	ENSP00000227378.3:p.Leu455=
ENST00000453788.6:c.1365G>T	ENSP00000404372.2:p.Leu455=
ENST00000524552.5:c.138G>T	ENSP00000435908.1:p.Leu46=
ENST00000526110.5:c.1308G>T	ENSP00000433584.1:p.Leu436=
ENST00000526686.1:c.21G>T	ENSP00000435019.1:p.Leu7=
ENST00000532091.1:n.1340G>T
ENST00000532636.5:c.1365G>T	ENSP00000437125.1:p.Leu455=
ENST00000533540.5:c.927G>T	ENSP00000437189.1:p.Leu309=
ENST00000534319.5:c.657G>T	ENSP00000433316.1:p.Leu219=
ENST00000534624.5:c.1365G>T	ENSP00000432083.1:p.Leu455=
NM_006597.5:c.1365G>T	NP_006588.1:p.Leu455=
NM_153201.3:c.1365G>T	NP_694881.1:p.Leu455=
XM_011542798.1:c.1365G>T	XP_011541100.1:p.Leu455=
NM_006597.6:c.1365G>T MANE Select	NP_006588.1:p.Leu455=
NM_153201.4:c.1365G>T	NP_694881.1:p.Leu455=