Canonical Allele Identifier: CA2066828457

Gene: HSPB8

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.119187078A= , CM000674.2:g.119187078A=	GRCh38
NC_000012.11:g.119624883A= , CM000674.1:g.119624883A=	GRCh37
NC_000012.10:g.118109266A=	NCBI36
NG_007953.2:g.13289A= , LRG_249:g.13289A=

Transcript Alleles

HGVS	Amino-acid Change
NM_014365.3:c.421A= MANE Select	NP_055180.1:p.Lys141=
ENST00000281938.7:c.421A= MANE Select	ENSP00000281938.3:p.Lys141=
NM_014365.2:c.421A= , LRG_249t1:c.421A=	NP_055180.1:p.Lys141=
ENST00000281938.6:c.421A=	ENSP00000281938.2:p.Lys141=
ENST00000541798.1:c.144A=
ENST00000542496.1:n.279A=
ENST00000674542.1:c.368-6621A=	ENSP00000502352.1:n.368-6621A=
ENST00000674715.1:n.594A=
ENST00000674763.1:c.54A=
ENST00000674852.1:c.54A=
ENST00000675110.1:c.54A=
ENST00000675211.1:c.54A=
ENST00000675573.1:c.54A=
ENST00000675900.1:n.21+5042A=
ENST00000676071.1:n.154A=
ENST00000676244.1:n.127A=