Canonical Allele Identifier: CA367765451
Gene: HSPB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.76303837A>T , CM000669.2:g.76303837A>T GRCh38
NC_000007.13:g.75933154A>T , CM000669.1:g.75933154A>T GRCh37
NC_000007.12:g.75771090A>T NCBI36
NG_008995.1:g.6280A>T , LRG_248:g.6280A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248553.7:c.400A>T MANE Select ENSP00000248553.6:p.Ile134Phe
ENST00000674547.1:c.400A>T ENSP00000502461.1:p.Ile134Phe
ENST00000674638.1:c.395A>T ENSP00000502651.1:p.His132Leu
ENST00000674650.1:c.365-147A>T ENSP00000501628.1:n.365-147A>T
ENST00000674965.1:c.*56A>T ENSP00000501765.1:n.*56A>T
ENST00000675134.1:c.400A>T ENSP00000501831.1:p.Ile134Phe
ENST00000675226.1:c.399A>T ENSP00000502510.1:p.Thr133=
ENST00000675417.1:n.633A>T
ENST00000675538.1:c.435A>T ENSP00000502495.1:p.Thr145=
ENST00000675906.1:c.400A>T ENSP00000502714.1:p.Ile134Phe
ENST00000676195.1:n.116A>T
ENST00000676231.1:c.430A>T ENSP00000502249.1:p.Ile144Phe
ENST00000248553.6:c.400A>T ENSP00000248553.6:p.Ile134Phe
ENST00000429938.1:c.-105A>T ENSP00000405285.1:n.-105A>T
ENST00000447574.1:c.*564A>T ENSP00000414357.1:n.*564A>T
NM_001540.3:c.400A>T , LRG_248t1:c.400A>T NP_001531.1:p.Ile134Phe
NM_001540.4:c.400A>T NP_001531.1:p.Ile134Phe
NM_001540.5:c.400A>T MANE Select NP_001531.1:p.Ile134Phe