Canonical Allele Identifier: CA1718331507
Gene: HSPB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.76304106C= , CM000669.2:g.76304106C= GRCh38
NC_000007.13:g.75933423C= , CM000669.1:g.75933423C= GRCh37
NC_000007.12:g.75771359C= NCBI36
NG_008995.1:g.6549C= , LRG_248:g.6549C=

Transcript Alleles

HGVS Amino-acid change
ENST00000248553.7:c.551C= MANE Select ENSP00000248553.6:p.Thr184=
ENST00000674547.1:c.*142C= ENSP00000502461.1:n.*142C=
ENST00000674638.1:c.*72C= ENSP00000502651.1:n.*72C=
ENST00000674650.1:c.*61C= ENSP00000501628.1:n.*61C=
ENST00000674965.1:c.*207C= ENSP00000501765.1:n.*207C=
ENST00000675134.1:c.530C= ENSP00000501831.1:p.Thr177=
ENST00000675226.1:c.*61C= ENSP00000502510.1:n.*61C=
ENST00000675417.1:n.902C=
ENST00000675538.1:c.*61C= ENSP00000502495.1:n.*61C=
ENST00000675906.1:c.*136C= ENSP00000502714.1:n.*136C=
ENST00000676231.1:c.581C= ENSP00000502249.1:p.Thr194=
ENST00000248553.6:c.551C= ENSP00000248553.6:p.Thr184=
ENST00000429938.1:c.47C= ENSP00000405285.1:p.Thr16=
ENST00000447574.1:c.*715C= ENSP00000414357.1:n.*715C=
NM_001540.3:c.551C= , LRG_248t1:c.551C= NP_001531.1:p.Thr184=
NM_001540.4:c.551C= NP_001531.1:p.Thr184=
NM_001540.5:c.551C= MANE Select NP_001531.1:p.Thr184=