Canonical Allele Identifier: CA386529568

Gene: HSPB8

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.119187079A>T , CM000674.2:g.119187079A>T	GRCh38
NC_000012.11:g.119624884A>T , CM000674.1:g.119624884A>T	GRCh37
NC_000012.10:g.118109267A>T	NCBI36
NG_007953.2:g.13290A>T , LRG_249:g.13290A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014365.3:c.422A>T MANE Select	NP_055180.1:p.Lys141Met
ENST00000281938.7:c.422A>T MANE Select	ENSP00000281938.3:p.Lys141Met
NM_014365.2:c.422A>T , LRG_249t1:c.422A>T	NP_055180.1:p.Lys141Met
ENST00000281938.6:c.422A>T	ENSP00000281938.2:p.Lys141Met
ENST00000541798.1:c.145A>T
ENST00000542496.1:n.280A>T
ENST00000674542.1:c.368-6620A>T	ENSP00000502352.1:n.368-6620A>T
ENST00000674715.1:n.595A>T
ENST00000674763.1:c.55A>T
ENST00000674852.1:c.55A>T
ENST00000675110.1:c.55A>T
ENST00000675211.1:c.55A>T
ENST00000675573.1:c.55A>T
ENST00000675900.1:n.21+5043A>T
ENST00000676071.1:n.155A>T
ENST00000676244.1:n.128A>T