Canonical Allele Identifier: CA1718331513
Gene: HSPB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.76304107C= , CM000669.2:g.76304107C= GRCh38
NC_000007.13:g.75933424C= , CM000669.1:g.75933424C= GRCh37
NC_000007.12:g.75771360C= NCBI36
NG_008995.1:g.6550C= , LRG_248:g.6550C=

Transcript Alleles

HGVS Amino-acid change
ENST00000248553.7:c.552C= MANE Select ENSP00000248553.6:p.Thr184=
ENST00000674547.1:c.*143C= ENSP00000502461.1:n.*143C=
ENST00000674638.1:c.*73C= ENSP00000502651.1:n.*73C=
ENST00000674650.1:c.*62C= ENSP00000501628.1:n.*62C=
ENST00000674965.1:c.*208C= ENSP00000501765.1:n.*208C=
ENST00000675134.1:c.531C= ENSP00000501831.1:p.Thr177=
ENST00000675226.1:c.*62C= ENSP00000502510.1:n.*62C=
ENST00000675417.1:n.903C=
ENST00000675538.1:c.*62C= ENSP00000502495.1:n.*62C=
ENST00000675906.1:c.*137C= ENSP00000502714.1:n.*137C=
ENST00000676231.1:c.582C= ENSP00000502249.1:p.Thr194=
ENST00000248553.6:c.552C= ENSP00000248553.6:p.Thr184=
ENST00000429938.1:c.48C= ENSP00000405285.1:p.Thr16=
ENST00000447574.1:c.*716C= ENSP00000414357.1:n.*716C=
NM_001540.3:c.552C= , LRG_248t1:c.552C= NP_001531.1:p.Thr184=
NM_001540.4:c.552C= NP_001531.1:p.Thr184=
NM_001540.5:c.552C= MANE Select NP_001531.1:p.Thr184=