Canonical Allele Identifier: CA482058247

Gene: HSPB8

Linked Data

• MyVariant Identifiers: chr12:g.119624885G>A (hg19)

Genomic Alleles

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

Transcript Alleles

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