Canonical Allele Identifier: CA1718330936

Gene: HSPB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303848C= , CM000669.2:g.76303848C=	GRCh38
NC_000007.13:g.75933165C= , CM000669.1:g.75933165C=	GRCh37
NC_000007.12:g.75771101C=	NCBI36
NG_008995.1:g.6291C= , LRG_248:g.6291C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.411C= MANE Select	ENSP00000248553.6:p.Cys137=
ENST00000674547.1:c.411C=	ENSP00000502461.1:p.Cys137=
ENST00000674638.1:c.406C=	ENSP00000502651.1:p.Leu136=
ENST00000674650.1:c.365-136C=	ENSP00000501628.1:n.365-136C=
ENST00000674965.1:c.*67C=	ENSP00000501765.1:n.*67C=
ENST00000675134.1:c.407+4C=	ENSP00000501831.1:n.407+4C=
ENST00000675226.1:c.410C=	ENSP00000502510.1:p.Ala137=
ENST00000675417.1:n.644C=
ENST00000675538.1:c.446C=	ENSP00000502495.1:p.Ala149=
ENST00000675906.1:c.411C=	ENSP00000502714.1:p.Cys137=
ENST00000676195.1:n.127C=
ENST00000676231.1:c.441C=	ENSP00000502249.1:p.Cys147=
ENST00000248553.6:c.411C=	ENSP00000248553.6:p.Cys137=
ENST00000429938.1:c.-94C=	ENSP00000405285.1:n.-94C=
ENST00000447574.1:c.*575C=	ENSP00000414357.1:n.*575C=
NM_001540.3:c.411C= , LRG_248t1:c.411C=	NP_001531.1:p.Cys137=
NM_001540.4:c.411C=	NP_001531.1:p.Cys137=
NM_001540.5:c.411C= MANE Select	NP_001531.1:p.Cys137=