Canonical Allele Identifier: CA383057329

Gene: HSPA8

Linked Data

• MyVariant Identifiers: chr11:g.122929466G>T (hg19) ; chr11:g.123058758G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058758G>T , CM000673.2:g.123058758G>T	GRCh38
NC_000011.9:g.122929466G>T , CM000673.1:g.122929466G>T	GRCh37
NC_000011.8:g.122434676G>T	NCBI36
NG_029473.1:g.8379C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1396C>A MANE Select	ENSP00000432083.1:p.Pro466Thr
ENST00000227378.7:c.1396C>A	ENSP00000227378.3:p.Pro466Thr
ENST00000453788.6:c.1387+9C>A	ENSP00000404372.2:n.1387+9C>A
ENST00000524552.5:c.169C>A	ENSP00000435908.1:p.Pro57Thr
ENST00000526110.5:c.1339C>A	ENSP00000433584.1:p.Pro447Thr
ENST00000526686.1:c.52C>A	ENSP00000435019.1:p.Pro18Thr
ENST00000532091.1:n.1371C>A
ENST00000532636.5:c.1396C>A	ENSP00000437125.1:p.Pro466Thr
ENST00000533540.5:c.958C>A	ENSP00000437189.1:p.Pro320Thr
ENST00000534319.5:c.688C>A	ENSP00000433316.1:p.Pro230Thr
ENST00000534624.5:c.1396C>A	ENSP00000432083.1:p.Pro466Thr
NM_006597.5:c.1396C>A	NP_006588.1:p.Pro466Thr
NM_153201.3:c.1387+9C>A	NP_694881.1:n.1387+9C>A
XM_011542798.1:c.1396C>A	XP_011541100.1:p.Pro466Thr
NM_006597.6:c.1396C>A MANE Select	NP_006588.1:p.Pro466Thr
NM_153201.4:c.1387+9C>A	NP_694881.1:n.1387+9C>A