Canonical Allele Identifier: CA2066828459

Gene: HSPB8

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.119187080G= , CM000674.2:g.119187080G=	GRCh38
NC_000012.11:g.119624885G= , CM000674.1:g.119624885G=	GRCh37
NC_000012.10:g.118109268G=	NCBI36
NG_007953.2:g.13291G= , LRG_249:g.13291G=

Transcript Alleles

HGVS	Amino-acid Change
NM_014365.3:c.423G= MANE Select	NP_055180.1:p.Lys141=
ENST00000281938.7:c.423G= MANE Select	ENSP00000281938.3:p.Lys141=
NM_014365.2:c.423G= , LRG_249t1:c.423G=	NP_055180.1:p.Lys141=
ENST00000281938.6:c.423G=	ENSP00000281938.2:p.Lys141=
ENST00000541798.1:c.146G=
ENST00000542496.1:n.281G=
ENST00000674542.1:c.368-6619G=	ENSP00000502352.1:n.368-6619G=
ENST00000674715.1:n.596G=
ENST00000674763.1:c.56G=
ENST00000674852.1:c.56G=
ENST00000675110.1:c.56G=
ENST00000675211.1:c.56G=
ENST00000675573.1:c.56G=
ENST00000675900.1:n.21+5044G=
ENST00000676071.1:n.156G=
ENST00000676244.1:n.129G=