Canonical Allele Identifier: CA2005597340

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059286_123059289delinsAAAG , CM000673.2:g.123059286_123059289delinsAAAG	GRCh38
NC_000011.9:g.122929994_122929997delinsAAAG , CM000673.1:g.122929994_122929997delinsAAAG	GRCh37
NC_000011.8:g.122435204_122435207delinsAAAG	NCBI36
NG_029473.1:g.7848_7851delinsCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1121-28_1121-25delinsCTTT MANE Select	ENSP00000432083.1:n.1121-28_1121-25delinsCTTT
ENST00000227378.7:c.1121-28_1121-25delinsCTTT	ENSP00000227378.3:n.1121-28_1121-25delinsCTTT
ENST00000453788.6:c.1121-28_1121-25delinsCTTT	ENSP00000404372.2:n.1121-28_1121-25delinsCTTT
ENST00000524552.5:c.-135_-132delinsCTTT	ENSP00000435908.1:n.-135_-132delinsCTTT
ENST00000526110.5:c.1064-28_1064-25delinsCTTT	ENSP00000433584.1:n.1064-28_1064-25delinsCTTT
ENST00000526862.1:n.399-28_399-25delinsCTTT
ENST00000527983.5:n.1453_1456delinsCTTT
ENST00000532091.1:n.868-28_868-25delinsCTTT
ENST00000532636.5:c.1121-28_1121-25delinsCTTT	ENSP00000437125.1:n.1121-28_1121-25delinsCTTT
ENST00000533238.5:n.381-186_381-183delinsCTTT
ENST00000533540.5:c.683-28_683-25delinsCTTT	ENSP00000437189.1:n.683-28_683-25delinsCTTT
ENST00000534319.5:c.413-28_413-25delinsCTTT	ENSP00000433316.1:n.413-28_413-25delinsCTTT
ENST00000534624.5:c.1121-28_1121-25delinsCTTT	ENSP00000432083.1:n.1121-28_1121-25delinsCTTT
NM_006597.5:c.1121-28_1121-25delinsCTTT	NP_006588.1:n.1121-28_1121-25delinsCTTT
NM_153201.3:c.1121-28_1121-25delinsCTTT	NP_694881.1:n.1121-28_1121-25delinsCTTT
XM_011542798.1:c.1121-28_1121-25delinsCTTT	XP_011541100.1:n.1121-28_1121-25delinsCTTT
NM_006597.6:c.1121-28_1121-25delinsCTTT MANE Select	NP_006588.1:n.1121-28_1121-25delinsCTTT
NM_153201.4:c.1121-28_1121-25delinsCTTT	NP_694881.1:n.1121-28_1121-25delinsCTTT