Canonical Allele Identifier: CA1718331501
Gene: HSPB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.76304103T= , CM000669.2:g.76304103T= GRCh38
NC_000007.13:g.75933420T= , CM000669.1:g.75933420T= GRCh37
NC_000007.12:g.75771356T= NCBI36
NG_008995.1:g.6546T= , LRG_248:g.6546T=

Transcript Alleles

HGVS Amino-acid change
ENST00000248553.7:c.548T= MANE Select ENSP00000248553.6:p.Val183=
ENST00000674547.1:c.*139T= ENSP00000502461.1:n.*139T=
ENST00000674638.1:c.*69T= ENSP00000502651.1:n.*69T=
ENST00000674650.1:c.*58T= ENSP00000501628.1:n.*58T=
ENST00000674965.1:c.*204T= ENSP00000501765.1:n.*204T=
ENST00000675134.1:c.527T= ENSP00000501831.1:p.Val176=
ENST00000675226.1:c.*58T= ENSP00000502510.1:n.*58T=
ENST00000675417.1:n.899T=
ENST00000675538.1:c.*58T= ENSP00000502495.1:n.*58T=
ENST00000675906.1:c.*133T= ENSP00000502714.1:n.*133T=
ENST00000676231.1:c.578T= ENSP00000502249.1:p.Val193=
ENST00000248553.6:c.548T= ENSP00000248553.6:p.Val183=
ENST00000429938.1:c.44T= ENSP00000405285.1:p.Val15=
ENST00000447574.1:c.*712T= ENSP00000414357.1:n.*712T=
NM_001540.3:c.548T= , LRG_248t1:c.548T= NP_001531.1:p.Val183=
NM_001540.4:c.548T= NP_001531.1:p.Val183=
NM_001540.5:c.548T= MANE Select NP_001531.1:p.Val183=