Canonical Allele Identifier: CA383058218

Gene: HSPA8

Linked Data

• MyVariant Identifiers: chr11:g.122929849A>G (hg19) ; chr11:g.123059141A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059141A>G , CM000673.2:g.123059141A>G	GRCh38
NC_000011.9:g.122929849A>G , CM000673.1:g.122929849A>G	GRCh37
NC_000011.8:g.122435059A>G	NCBI36
NG_029473.1:g.7996T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1241T>C MANE Select	ENSP00000432083.1:p.Ile414Thr
ENST00000227378.7:c.1241T>C	ENSP00000227378.3:p.Ile414Thr
ENST00000453788.6:c.1241T>C	ENSP00000404372.2:p.Ile414Thr
ENST00000524552.5:c.14T>C	ENSP00000435908.1:p.Ile5Thr
ENST00000526110.5:c.1184T>C	ENSP00000433584.1:p.Ile395Thr
ENST00000532091.1:n.988T>C
ENST00000532636.5:c.1241T>C	ENSP00000437125.1:p.Ile414Thr
ENST00000533238.5:n.381-38T>C
ENST00000533540.5:c.803T>C	ENSP00000437189.1:p.Ile268Thr
ENST00000534319.5:c.533T>C	ENSP00000433316.1:p.Ile178Thr
ENST00000534624.5:c.1241T>C	ENSP00000432083.1:p.Ile414Thr
NM_006597.5:c.1241T>C	NP_006588.1:p.Ile414Thr
NM_153201.3:c.1241T>C	NP_694881.1:p.Ile414Thr
XM_011542798.1:c.1241T>C	XP_011541100.1:p.Ile414Thr
NM_006597.6:c.1241T>C MANE Select	NP_006588.1:p.Ile414Thr
NM_153201.4:c.1241T>C	NP_694881.1:p.Ile414Thr