Canonical Allele Identifier: CA383057023

Gene: HSPA8

Linked Data

• MyVariant Identifiers: chr11:g.122929348T>G (hg19) ; chr11:g.123058640T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058640T>G , CM000673.2:g.123058640T>G	GRCh38
NC_000011.9:g.122929348T>G , CM000673.1:g.122929348T>G	GRCh37
NC_000011.8:g.122434558T>G	NCBI36
NG_029473.1:g.8497A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1514A>C MANE Select	ENSP00000432083.1:p.Asn505Thr
ENST00000227378.7:c.1514A>C	ENSP00000227378.3:p.Asn505Thr
ENST00000453788.6:c.1387+127A>C	ENSP00000404372.2:n.1387+127A>C
ENST00000524552.5:c.287A>C	ENSP00000435908.1:p.Asn96Thr
ENST00000526110.5:c.1457A>C	ENSP00000433584.1:p.Asn486Thr
ENST00000526686.1:c.170A>C	ENSP00000435019.1:p.Asn57Thr
ENST00000532091.1:n.1489A>C
ENST00000532636.5:c.1514A>C	ENSP00000437125.1:p.Asn505Thr
ENST00000533540.5:c.1076A>C	ENSP00000437189.1:p.Asn359Thr
ENST00000534319.5:c.806A>C	ENSP00000433316.1:p.Asn269Thr
ENST00000534624.5:c.1514A>C	ENSP00000432083.1:p.Asn505Thr
NM_006597.5:c.1514A>C	NP_006588.1:p.Asn505Thr
NM_153201.3:c.1387+127A>C	NP_694881.1:n.1387+127A>C
XM_011542798.1:c.1514A>C	XP_011541100.1:p.Asn505Thr
NM_006597.6:c.1514A>C MANE Select	NP_006588.1:p.Asn505Thr
NM_153201.4:c.1387+127A>C	NP_694881.1:n.1387+127A>C