Canonical Allele Identifier: CA383057445

Gene: HSPA8

Linked Data

• MyVariant Identifiers: chr11:g.122929516A>T (hg19) ; chr11:g.123058808A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058808A>T , CM000673.2:g.123058808A>T	GRCh38
NC_000011.9:g.122929516A>T , CM000673.1:g.122929516A>T	GRCh37
NC_000011.8:g.122434726A>T	NCBI36
NG_029473.1:g.8329T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1346T>A MANE Select	ENSP00000432083.1:p.Met449Lys
ENST00000227378.7:c.1346T>A	ENSP00000227378.3:p.Met449Lys
ENST00000453788.6:c.1346T>A	ENSP00000404372.2:p.Met449Lys
ENST00000524552.5:c.119T>A	ENSP00000435908.1:p.Met40Lys
ENST00000526110.5:c.1289T>A	ENSP00000433584.1:p.Met430Lys
ENST00000526686.1:c.2T>A	ENSP00000435019.1:p.Met1Lys
ENST00000532091.1:n.1321T>A
ENST00000532636.5:c.1346T>A	ENSP00000437125.1:p.Met449Lys
ENST00000533238.5:n.448T>A
ENST00000533540.5:c.908T>A	ENSP00000437189.1:p.Met303Lys
ENST00000534319.5:c.638T>A	ENSP00000433316.1:p.Met213Lys
ENST00000534624.5:c.1346T>A	ENSP00000432083.1:p.Met449Lys
NM_006597.5:c.1346T>A	NP_006588.1:p.Met449Lys
NM_153201.3:c.1346T>A	NP_694881.1:p.Met449Lys
XM_011542798.1:c.1346T>A	XP_011541100.1:p.Met449Lys
NM_006597.6:c.1346T>A MANE Select	NP_006588.1:p.Met449Lys
NM_153201.4:c.1346T>A	NP_694881.1:p.Met449Lys