Canonical Allele Identifier: CA367765318
Gene: HSPB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.76303813G>T , CM000669.2:g.76303813G>T GRCh38
NC_000007.13:g.75933130G>T , CM000669.1:g.75933130G>T GRCh37
NC_000007.12:g.75771066G>T NCBI36
NG_008995.1:g.6256G>T , LRG_248:g.6256G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248553.7:c.376G>T MANE Select ENSP00000248553.6:p.Glu126Ter
ENST00000674547.1:c.376G>T ENSP00000502461.1:p.Glu126Ter
ENST00000674638.1:c.371G>T ENSP00000502651.1:p.Gly124Val
ENST00000674650.1:c.365-171G>T ENSP00000501628.1:n.365-171G>T
ENST00000674965.1:c.*32G>T ENSP00000501765.1:n.*32G>T
ENST00000675134.1:c.376G>T ENSP00000501831.1:p.Glu126Ter
ENST00000675226.1:c.375G>T ENSP00000502510.1:p.Arg125Ser
ENST00000675417.1:n.609G>T
ENST00000675538.1:c.411G>T ENSP00000502495.1:p.Arg137Ser
ENST00000675906.1:c.376G>T ENSP00000502714.1:p.Glu126Ter
ENST00000676195.1:n.92G>T
ENST00000676231.1:c.406G>T ENSP00000502249.1:p.Glu136Ter
ENST00000248553.6:c.376G>T ENSP00000248553.6:p.Glu126Ter
ENST00000429938.1:c.-129G>T ENSP00000405285.1:n.-129G>T
ENST00000447574.1:c.*540G>T ENSP00000414357.1:n.*540G>T
NM_001540.3:c.376G>T , LRG_248t1:c.376G>T NP_001531.1:p.Glu126Ter
NM_001540.4:c.376G>T NP_001531.1:p.Glu126Ter
NM_001540.5:c.376G>T MANE Select NP_001531.1:p.Glu126Ter