Canonical Allele Identifier: CA2066828475

Gene: HSPB8

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.119187115_119187116delinsAG , CM000674.2:g.119187115_119187116delinsAG	GRCh38
NC_000012.11:g.119624920_119624921delinsAG , CM000674.1:g.119624920_119624921delinsAG	GRCh37
NC_000012.10:g.118109303_118109304delinsAG	NCBI36
NG_007953.2:g.13326_13327delinsAG , LRG_249:g.13326_13327delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281938.7:c.431+27_431+28delinsAG MANE Select	ENSP00000281938.3:n.431+27_431+28delinsAG
ENST00000674542.1:c.368-6584_368-6583delinsAG	ENSP00000502352.1:n.368-6584_368-6583delinsAG
ENST00000674715.1:n.604+27_604+28delinsAG
ENST00000674763.1:c.64+27_64+28delinsAG
ENST00000674852.1:c.64+27_64+28delinsAG
ENST00000675110.1:c.64+27_64+28delinsAG
ENST00000675211.1:c.64+27_64+28delinsAG
ENST00000675573.1:c.64+27_64+28delinsAG
ENST00000675900.1:n.21+5079_21+5080delinsAG
ENST00000676071.1:n.164+27_164+28delinsAG
ENST00000676244.1:n.137+27_137+28delinsAG
ENST00000281938.6:c.431+27_431+28delinsAG	ENSP00000281938.2:n.431+27_431+28delinsAG
ENST00000541798.1:c.154+27_154+28delinsAG
ENST00000542496.1:n.289+27_289+28delinsAG
NM_014365.2:c.431+27_431+28delinsAG , LRG_249t1:c.431+27_431+28delinsAG	NP_055180.1:n.431+27_431+28delinsAG
NM_014365.3:c.431+27_431+28delinsAG MANE Select	NP_055180.1:n.431+27_431+28delinsAG