Canonical Allele Identifier: CA2005595564

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058767_123058769delinsCTG , CM000673.2:g.123058767_123058769delinsCTG	GRCh38
NC_000011.9:g.122929475_122929477delinsCTG , CM000673.1:g.122929475_122929477delinsCTG	GRCh37
NC_000011.8:g.122434685_122434687delinsCTG	NCBI36
NG_029473.1:g.8368_8370delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1385_1387delinsCAG MANE Select	ENSP00000432083.1:p.Thr462=
ENST00000227378.7:c.1385_1387delinsCAG	ENSP00000227378.3:p.Thr462=
ENST00000453788.6:c.1385_1387delinsCAG	ENSP00000404372.2:p.Thr462=
ENST00000524552.5:c.158_160delinsCAG	ENSP00000435908.1:p.Thr53=
ENST00000526110.5:c.1328_1330delinsCAG	ENSP00000433584.1:p.Thr443=
ENST00000526686.1:c.41_43delinsCAG	ENSP00000435019.1:p.Thr14=
ENST00000532091.1:n.1360_1362delinsCAG
ENST00000532636.5:c.1385_1387delinsCAG	ENSP00000437125.1:p.Thr462=
ENST00000533540.5:c.947_949delinsCAG	ENSP00000437189.1:p.Thr316=
ENST00000534319.5:c.677_679delinsCAG	ENSP00000433316.1:p.Thr226=
ENST00000534624.5:c.1385_1387delinsCAG	ENSP00000432083.1:p.Thr462=
NM_006597.5:c.1385_1387delinsCAG	NP_006588.1:p.Thr462=
NM_153201.3:c.1385_1387delinsCAG	NP_694881.1:p.Thr462=
XM_011542798.1:c.1385_1387delinsCAG	XP_011541100.1:p.Thr462=
NM_006597.6:c.1385_1387delinsCAG MANE Select	NP_006588.1:p.Thr462=
NM_153201.4:c.1385_1387delinsCAG	NP_694881.1:p.Thr462=