Canonical Allele Identifier: CA383057400

Gene: HSPA8

Linked Data

• MyVariant Identifiers: chr11:g.122929499G>T (hg19) ; chr11:g.123058791G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058791G>T , CM000673.2:g.123058791G>T	GRCh38
NC_000011.9:g.122929499G>T , CM000673.1:g.122929499G>T	GRCh37
NC_000011.8:g.122434709G>T	NCBI36
NG_029473.1:g.8346C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1363C>A MANE Select	ENSP00000432083.1:p.Leu455Met
ENST00000227378.7:c.1363C>A	ENSP00000227378.3:p.Leu455Met
ENST00000453788.6:c.1363C>A	ENSP00000404372.2:p.Leu455Met
ENST00000524552.5:c.136C>A	ENSP00000435908.1:p.Leu46Met
ENST00000526110.5:c.1306C>A	ENSP00000433584.1:p.Leu436Met
ENST00000526686.1:c.19C>A	ENSP00000435019.1:p.Leu7Met
ENST00000532091.1:n.1338C>A
ENST00000532636.5:c.1363C>A	ENSP00000437125.1:p.Leu455Met
ENST00000533238.5:n.465C>A
ENST00000533540.5:c.925C>A	ENSP00000437189.1:p.Leu309Met
ENST00000534319.5:c.655C>A	ENSP00000433316.1:p.Leu219Met
ENST00000534624.5:c.1363C>A	ENSP00000432083.1:p.Leu455Met
NM_006597.5:c.1363C>A	NP_006588.1:p.Leu455Met
NM_153201.3:c.1363C>A	NP_694881.1:p.Leu455Met
XM_011542798.1:c.1363C>A	XP_011541100.1:p.Leu455Met
NM_006597.6:c.1363C>A MANE Select	NP_006588.1:p.Leu455Met
NM_153201.4:c.1363C>A	NP_694881.1:p.Leu455Met