Canonical Allele Identifier: CA1718328909

Gene: HSPB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76302888_76302922delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG , CM000669.2:g.76302888_76302922delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG	GRCh38
NC_000007.13:g.75932205_75932239delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG , CM000669.1:g.75932205_75932239delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG	GRCh37
NC_000007.12:g.75770141_75770175delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG	NCBI36
NG_008995.1:g.5331_5365delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG , LRG_248:g.5331_5365delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000248553.7:c.176_210delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG MANE Select	ENSP00000248553.6:p.Pro59=
ENST00000674547.1:c.176_210delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG	ENSP00000502461.1:p.Pro59=
ENST00000674560.1:n.216_250delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG
ENST00000674638.1:c.176_210delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG	ENSP00000502651.1:p.Pro59=
ENST00000674650.1:c.176_210delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG	ENSP00000501628.1:p.Pro59=
ENST00000674965.1:c.176_210delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG	ENSP00000501765.1:p.Pro59=
ENST00000675134.1:c.176_210delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG	ENSP00000501831.1:p.Pro59=
ENST00000675226.1:c.176_210delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG	ENSP00000502510.1:p.Pro59=
ENST00000675488.1:n.216_250delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG
ENST00000675538.1:c.176_210delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG	ENSP00000502495.1:p.Pro59=
ENST00000675624.1:n.216_250delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG
ENST00000675733.1:n.216_250delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG
ENST00000675906.1:c.176_210delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG	ENSP00000502714.1:p.Pro59=
ENST00000676231.1:c.176_210delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG	ENSP00000502249.1:p.Pro59=
ENST00000676398.1:n.216_250delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG
ENST00000248553.6:c.176_210delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG	ENSP00000248553.6:p.Pro59=
ENST00000447574.1:c.176_210delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG	ENSP00000414357.1:p.Pro59=
NM_001540.3:c.176_210delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG , LRG_248t1:c.176_210delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG	NP_001531.1:p.Pro59=
NM_001540.4:c.176_210delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG	NP_001531.1:p.Pro59=
NM_001540.5:c.176_210delinsCCCCCGCCGCCATCGAGAGCCCCGCAGTGGCCGCG MANE Select	NP_001531.1:p.Pro59=