Canonical Allele Identifier: CA1718331504
Gene: HSPB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.76304105A= , CM000669.2:g.76304105A= GRCh38
NC_000007.13:g.75933422A= , CM000669.1:g.75933422A= GRCh37
NC_000007.12:g.75771358A= NCBI36
NG_008995.1:g.6548A= , LRG_248:g.6548A=

Transcript Alleles

HGVS Amino-acid change
ENST00000248553.7:c.550A= MANE Select ENSP00000248553.6:p.Thr184=
ENST00000674547.1:c.*141A= ENSP00000502461.1:n.*141A=
ENST00000674638.1:c.*71A= ENSP00000502651.1:n.*71A=
ENST00000674650.1:c.*60A= ENSP00000501628.1:n.*60A=
ENST00000674965.1:c.*206A= ENSP00000501765.1:n.*206A=
ENST00000675134.1:c.529A= ENSP00000501831.1:p.Thr177=
ENST00000675226.1:c.*60A= ENSP00000502510.1:n.*60A=
ENST00000675417.1:n.901A=
ENST00000675538.1:c.*60A= ENSP00000502495.1:n.*60A=
ENST00000675906.1:c.*135A= ENSP00000502714.1:n.*135A=
ENST00000676231.1:c.580A= ENSP00000502249.1:p.Thr194=
ENST00000248553.6:c.550A= ENSP00000248553.6:p.Thr184=
ENST00000429938.1:c.46A= ENSP00000405285.1:p.Thr16=
ENST00000447574.1:c.*714A= ENSP00000414357.1:n.*714A=
NM_001540.3:c.550A= , LRG_248t1:c.550A= NP_001531.1:p.Thr184=
NM_001540.4:c.550A= NP_001531.1:p.Thr184=
NM_001540.5:c.550A= MANE Select NP_001531.1:p.Thr184=