Canonical Allele Identifier: CA1718331518
Gene: HSPB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.76304109T= , CM000669.2:g.76304109T= GRCh38
NC_000007.13:g.75933426T= , CM000669.1:g.75933426T= GRCh37
NC_000007.12:g.75771362T= NCBI36
NG_008995.1:g.6552T= , LRG_248:g.6552T=

Transcript Alleles

HGVS Amino-acid change
ENST00000248553.7:c.554T= MANE Select ENSP00000248553.6:p.Phe185=
ENST00000674547.1:c.*145T= ENSP00000502461.1:n.*145T=
ENST00000674638.1:c.*75T= ENSP00000502651.1:n.*75T=
ENST00000674650.1:c.*64T= ENSP00000501628.1:n.*64T=
ENST00000674965.1:c.*210T= ENSP00000501765.1:n.*210T=
ENST00000675134.1:c.533T= ENSP00000501831.1:p.Phe178=
ENST00000675226.1:c.*64T= ENSP00000502510.1:n.*64T=
ENST00000675417.1:n.905T=
ENST00000675538.1:c.*64T= ENSP00000502495.1:n.*64T=
ENST00000675906.1:c.*139T= ENSP00000502714.1:n.*139T=
ENST00000676231.1:c.584T= ENSP00000502249.1:p.Phe195=
ENST00000248553.6:c.554T= ENSP00000248553.6:p.Phe185=
ENST00000429938.1:c.50T= ENSP00000405285.1:p.Phe17=
ENST00000447574.1:c.*718T= ENSP00000414357.1:n.*718T=
NM_001540.3:c.554T= , LRG_248t1:c.554T= NP_001531.1:p.Phe185=
NM_001540.4:c.554T= NP_001531.1:p.Phe185=
NM_001540.5:c.554T= MANE Select NP_001531.1:p.Phe185=