Canonical Allele Identifier: CA383057133

Gene: HSPA8

Linked Data

• COSMIC: COSM5953993
• MyVariant Identifiers: chr11:g.122929378G>T (hg19) ; chr11:g.123058670G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058670G>T , CM000673.2:g.123058670G>T	GRCh38
NC_000011.9:g.122929378G>T , CM000673.1:g.122929378G>T	GRCh37
NC_000011.8:g.122434588G>T	NCBI36
NG_029473.1:g.8467C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1484C>A MANE Select	ENSP00000432083.1:p.Thr495Lys
ENST00000227378.7:c.1484C>A	ENSP00000227378.3:p.Thr495Lys
ENST00000453788.6:c.1387+97C>A	ENSP00000404372.2:n.1387+97C>A
ENST00000524552.5:c.257C>A	ENSP00000435908.1:p.Thr86Lys
ENST00000526110.5:c.1427C>A	ENSP00000433584.1:p.Thr476Lys
ENST00000526686.1:c.140C>A	ENSP00000435019.1:p.Thr47Lys
ENST00000532091.1:n.1459C>A
ENST00000532636.5:c.1484C>A	ENSP00000437125.1:p.Thr495Lys
ENST00000533540.5:c.1046C>A	ENSP00000437189.1:p.Thr349Lys
ENST00000534319.5:c.776C>A	ENSP00000433316.1:p.Thr259Lys
ENST00000534624.5:c.1484C>A	ENSP00000432083.1:p.Thr495Lys
NM_006597.5:c.1484C>A	NP_006588.1:p.Thr495Lys
NM_153201.3:c.1387+97C>A	NP_694881.1:n.1387+97C>A
XM_011542798.1:c.1484C>A	XP_011541100.1:p.Thr495Lys
NM_006597.6:c.1484C>A MANE Select	NP_006588.1:p.Thr495Lys
NM_153201.4:c.1387+97C>A	NP_694881.1:n.1387+97C>A