Canonical Allele Identifier: CA367765280
Gene: HSPB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.76303807C>A , CM000669.2:g.76303807C>A GRCh38
NC_000007.13:g.75933124C>A , CM000669.1:g.75933124C>A GRCh37
NC_000007.12:g.75771060C>A NCBI36
NG_008995.1:g.6250C>A , LRG_248:g.6250C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000248553.7:c.370C>A MANE Select ENSP00000248553.6:p.His124Asn
ENST00000674547.1:c.370C>A ENSP00000502461.1:p.His124Asn
ENST00000674638.1:c.365C>A ENSP00000502651.1:p.Ala122Glu
ENST00000674650.1:c.365-177C>A ENSP00000501628.1:n.365-177C>A
ENST00000674965.1:c.*26C>A ENSP00000501765.1:n.*26C>A
ENST00000675134.1:c.370C>A ENSP00000501831.1:p.His124Asn
ENST00000675226.1:c.369C>A ENSP00000502510.1:p.Asp123Glu
ENST00000675417.1:n.603C>A
ENST00000675538.1:c.405C>A ENSP00000502495.1:p.Ser135Arg
ENST00000675906.1:c.370C>A ENSP00000502714.1:p.His124Asn
ENST00000676195.1:n.86C>A
ENST00000676231.1:c.400C>A ENSP00000502249.1:p.His134Asn
ENST00000248553.6:c.370C>A ENSP00000248553.6:p.His124Asn
ENST00000429938.1:c.-135C>A ENSP00000405285.1:n.-135C>A
ENST00000447574.1:c.*534C>A ENSP00000414357.1:n.*534C>A
NM_001540.3:c.370C>A , LRG_248t1:c.370C>A NP_001531.1:p.His124Asn
NM_001540.4:c.370C>A NP_001531.1:p.His124Asn
NM_001540.5:c.370C>A MANE Select NP_001531.1:p.His124Asn