Canonical Allele Identifier: CA1718330905

Gene: HSPB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303843C= , CM000669.2:g.76303843C=	GRCh38
NC_000007.13:g.75933160C= , CM000669.1:g.75933160C=	GRCh37
NC_000007.12:g.75771096C=	NCBI36
NG_008995.1:g.6286C= , LRG_248:g.6286C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001540.5:c.406C= MANE Select	NP_001531.1:p.Arg136=
ENST00000248553.7:c.406C= MANE Select	ENSP00000248553.6:p.Arg136=
NM_001540.3:c.406C= , LRG_248t1:c.406C=	NP_001531.1:p.Arg136=
NM_001540.4:c.406C=	NP_001531.1:p.Arg136=
ENST00000248553.6:c.406C=	ENSP00000248553.6:p.Arg136=
ENST00000429938.1:c.-99C=	ENSP00000405285.1:n.-99C=
ENST00000447574.1:c.*570C=	ENSP00000414357.1:n.*570C=
ENST00000674547.1:c.406C=	ENSP00000502461.1:p.Arg136=
ENST00000674638.1:c.401C=	ENSP00000502651.1:p.Pro134=
ENST00000674650.1:c.365-141C=	ENSP00000501628.1:n.365-141C=
ENST00000674965.1:c.*62C=	ENSP00000501765.1:n.*62C=
ENST00000675134.1:c.406C=	ENSP00000501831.1:p.Arg136=
ENST00000675226.1:c.405C=	ENSP00000502510.1:p.Pro135=
ENST00000675417.1:n.639C=
ENST00000675538.1:c.441C=	ENSP00000502495.1:p.Pro147=
ENST00000675906.1:c.406C=	ENSP00000502714.1:p.Arg136=
ENST00000676195.1:n.122C=
ENST00000676231.1:c.436C=	ENSP00000502249.1:p.Arg146=