Canonical Allele Identifier: CA1718330900

Gene: HSPB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303841C= , CM000669.2:g.76303841C=	GRCh38
NC_000007.13:g.75933158C= , CM000669.1:g.75933158C=	GRCh37
NC_000007.12:g.75771094C=	NCBI36
NG_008995.1:g.6284C= , LRG_248:g.6284C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.404C= MANE Select	ENSP00000248553.6:p.Ser135=
ENST00000674547.1:c.404C=	ENSP00000502461.1:p.Ser135=
ENST00000674638.1:c.399C=	ENSP00000502651.1:p.Leu133=
ENST00000674650.1:c.365-143C=	ENSP00000501628.1:n.365-143C=
ENST00000674965.1:c.*60C=	ENSP00000501765.1:n.*60C=
ENST00000675134.1:c.404C=	ENSP00000501831.1:p.Ser135=
ENST00000675226.1:c.403C=	ENSP00000502510.1:p.Pro135=
ENST00000675417.1:n.637C=
ENST00000675538.1:c.439C=	ENSP00000502495.1:p.Pro147=
ENST00000675906.1:c.404C=	ENSP00000502714.1:p.Ser135=
ENST00000676195.1:n.120C=
ENST00000676231.1:c.434C=	ENSP00000502249.1:p.Ser145=
ENST00000248553.6:c.404C=	ENSP00000248553.6:p.Ser135=
ENST00000429938.1:c.-101C=	ENSP00000405285.1:n.-101C=
ENST00000447574.1:c.*568C=	ENSP00000414357.1:n.*568C=
NM_001540.3:c.404C= , LRG_248t1:c.404C=	NP_001531.1:p.Ser135=
NM_001540.4:c.404C=	NP_001531.1:p.Ser135=
NM_001540.5:c.404C= MANE Select	NP_001531.1:p.Ser135=