Canonical Allele Identifier: CA2005596439

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059013_123059020delinsTTTATCTG , CM000673.2:g.123059013_123059020delinsTTTATCTG	GRCh38
NC_000011.9:g.122929721_122929728delinsTTTATCTG , CM000673.1:g.122929721_122929728delinsTTTATCTG	GRCh37
NC_000011.8:g.122434931_122434938delinsTTTATCTG	NCBI36
NG_029473.1:g.8117_8124delinsCAGATAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1323+39_1323+46delinsCAGATAAA MANE Select	ENSP00000432083.1:n.1323+39_1323+46delinsCAGATAAA
ENST00000227378.7:c.1323+39_1323+46delinsCAGATAAA	ENSP00000227378.3:n.1323+39_1323+46delinsCAGATAAA
ENST00000453788.6:c.1323+39_1323+46delinsCAGATAAA	ENSP00000404372.2:n.1323+39_1323+46delinsCAGATAAA
ENST00000524552.5:c.96+39_96+46delinsCAGATAAA	ENSP00000435908.1:n.96+39_96+46delinsCAGATAAA
ENST00000526110.5:c.1266+39_1266+46delinsCAGATAAA	ENSP00000433584.1:n.1266+39_1266+46delinsCAGATAAA
ENST00000526686.1:c.-211_-204delinsCAGATAAA	ENSP00000435019.1:n.-211_-204delinsCAGATAAA
ENST00000532091.1:n.1109_1116delinsCAGATAAA
ENST00000532636.5:c.1323+39_1323+46delinsCAGATAAA	ENSP00000437125.1:n.1323+39_1323+46delinsCAGATAAA
ENST00000533238.5:n.425+39_425+46delinsCAGATAAA
ENST00000533540.5:c.885+39_885+46delinsCAGATAAA	ENSP00000437189.1:n.885+39_885+46delinsCAGATAAA
ENST00000534319.5:c.615+39_615+46delinsCAGATAAA	ENSP00000433316.1:n.615+39_615+46delinsCAGATAAA
ENST00000534624.5:c.1323+39_1323+46delinsCAGATAAA	ENSP00000432083.1:n.1323+39_1323+46delinsCAGATAAA
NM_006597.5:c.1323+39_1323+46delinsCAGATAAA	NP_006588.1:n.1323+39_1323+46delinsCAGATAAA
NM_153201.3:c.1323+39_1323+46delinsCAGATAAA	NP_694881.1:n.1323+39_1323+46delinsCAGATAAA
XM_011542798.1:c.1323+39_1323+46delinsCAGATAAA	XP_011541100.1:n.1323+39_1323+46delinsCAGATAAA
NM_006597.6:c.1323+39_1323+46delinsCAGATAAA MANE Select	NP_006588.1:n.1323+39_1323+46delinsCAGATAAA
NM_153201.4:c.1323+39_1323+46delinsCAGATAAA	NP_694881.1:n.1323+39_1323+46delinsCAGATAAA