Canonical Allele Identifier: CA2005596366

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058998_123059015delinsCAGTCAAGACTTCCCTTT , CM000673.2:g.123058998_123059015delinsCAGTCAAGACTTCCCTTT	GRCh38
NC_000011.9:g.122929706_122929723delinsCAGTCAAGACTTCCCTTT , CM000673.1:g.122929706_122929723delinsCAGTCAAGACTTCCCTTT	GRCh37
NC_000011.8:g.122434916_122434933delinsCAGTCAAGACTTCCCTTT	NCBI36
NG_029473.1:g.8122_8139delinsAAAGGGAAGTCTTGACTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1323+44_1323+61delinsAAAGGGAAGTCTTGACTG MANE Select	ENSP00000432083.1:n.1323+44_1323+61delinsAAAGGGAAGTCTTGACTG
ENST00000227378.7:c.1323+44_1323+61delinsAAAGGGAAGTCTTGACTG	ENSP00000227378.3:n.1323+44_1323+61delinsAAAGGGAAGTCTTGACTG
ENST00000453788.6:c.1323+44_1323+61delinsAAAGGGAAGTCTTGACTG	ENSP00000404372.2:n.1323+44_1323+61delinsAAAGGGAAGTCTTGACTG
ENST00000524552.5:c.96+44_96+61delinsAAAGGGAAGTCTTGACTG	ENSP00000435908.1:n.96+44_96+61delinsAAAGGGAAGTCTTGACTG
ENST00000526110.5:c.1266+44_1266+61delinsAAAGGGAAGTCTTGACTG	ENSP00000433584.1:n.1266+44_1266+61delinsAAAGGGAAGTCTTGACTG
ENST00000526686.1:c.-206_-189delinsAAAGGGAAGTCTTGACTG	ENSP00000435019.1:n.-206_-189delinsAAAGGGAAGTCTTGACTG
ENST00000532091.1:n.1114_1131delinsAAAGGGAAGTCTTGACTG
ENST00000532636.5:c.1323+44_1323+61delinsAAAGGGAAGTCTTGACTG	ENSP00000437125.1:n.1323+44_1323+61delinsAAAGGGAAGTCTTGACTG
ENST00000533238.5:n.425+44_425+61delinsAAAGGGAAGTCTTGACTG
ENST00000533540.5:c.885+44_885+61delinsAAAGGGAAGTCTTGACTG	ENSP00000437189.1:n.885+44_885+61delinsAAAGGGAAGTCTTGACTG
ENST00000534319.5:c.615+44_615+61delinsAAAGGGAAGTCTTGACTG	ENSP00000433316.1:n.615+44_615+61delinsAAAGGGAAGTCTTGACTG
ENST00000534624.5:c.1323+44_1323+61delinsAAAGGGAAGTCTTGACTG	ENSP00000432083.1:n.1323+44_1323+61delinsAAAGGGAAGTCTTGACTG
NM_006597.5:c.1323+44_1323+61delinsAAAGGGAAGTCTTGACTG	NP_006588.1:n.1323+44_1323+61delinsAAAGGGAAGTCTTGACTG
NM_153201.3:c.1323+44_1323+61delinsAAAGGGAAGTCTTGACTG	NP_694881.1:n.1323+44_1323+61delinsAAAGGGAAGTCTTGACTG
XM_011542798.1:c.1323+44_1323+61delinsAAAGGGAAGTCTTGACTG	XP_011541100.1:n.1323+44_1323+61delinsAAAGGGAAGTCTTGACTG
NM_006597.6:c.1323+44_1323+61delinsAAAGGGAAGTCTTGACTG MANE Select	NP_006588.1:n.1323+44_1323+61delinsAAAGGGAAGTCTTGACTG
NM_153201.4:c.1323+44_1323+61delinsAAAGGGAAGTCTTGACTG	NP_694881.1:n.1323+44_1323+61delinsAAAGGGAAGTCTTGACTG