Canonical Allele Identifier: CA1718330826

Gene: HSPB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303814A= , CM000669.2:g.76303814A=	GRCh38
NC_000007.13:g.75933131A= , CM000669.1:g.75933131A=	GRCh37
NC_000007.12:g.75771067A=	NCBI36
NG_008995.1:g.6257A= , LRG_248:g.6257A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.377A= MANE Select	ENSP00000248553.6:p.Glu126=
ENST00000674547.1:c.377A=	ENSP00000502461.1:p.Glu126=
ENST00000674638.1:c.372A=	ENSP00000502651.1:p.Gly124=
ENST00000674650.1:c.365-170A=	ENSP00000501628.1:n.365-170A=
ENST00000674965.1:c.*33A=	ENSP00000501765.1:n.*33A=
ENST00000675134.1:c.377A=	ENSP00000501831.1:p.Glu126=
ENST00000675226.1:c.376A=	ENSP00000502510.1:p.Ser126=
ENST00000675417.1:n.610A=
ENST00000675538.1:c.412A=	ENSP00000502495.1:p.Ser138=
ENST00000675906.1:c.377A=	ENSP00000502714.1:p.Glu126=
ENST00000676195.1:n.93A=
ENST00000676231.1:c.407A=	ENSP00000502249.1:p.Glu136=
ENST00000248553.6:c.377A=	ENSP00000248553.6:p.Glu126=
ENST00000429938.1:c.-128A=	ENSP00000405285.1:n.-128A=
ENST00000447574.1:c.*541A=	ENSP00000414357.1:n.*541A=
NM_001540.3:c.377A= , LRG_248t1:c.377A=	NP_001531.1:p.Glu126=
NM_001540.4:c.377A=	NP_001531.1:p.Glu126=
NM_001540.5:c.377A= MANE Select	NP_001531.1:p.Glu126=