Canonical Allele Identifier: CA1718331532
Gene: HSPB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.76304110C= , CM000669.2:g.76304110C= GRCh38
NC_000007.13:g.75933427C= , CM000669.1:g.75933427C= GRCh37
NC_000007.12:g.75771363C= NCBI36
NG_008995.1:g.6553C= , LRG_248:g.6553C=

Transcript Alleles

HGVS Amino-acid change
ENST00000248553.7:c.555C= MANE Select ENSP00000248553.6:p.Phe185=
ENST00000674547.1:c.*146C= ENSP00000502461.1:n.*146C=
ENST00000674638.1:c.*76C= ENSP00000502651.1:n.*76C=
ENST00000674650.1:c.*65C= ENSP00000501628.1:n.*65C=
ENST00000674965.1:c.*211C= ENSP00000501765.1:n.*211C=
ENST00000675134.1:c.534C= ENSP00000501831.1:p.Phe178=
ENST00000675226.1:c.*65C= ENSP00000502510.1:n.*65C=
ENST00000675417.1:n.906C=
ENST00000675538.1:c.*65C= ENSP00000502495.1:n.*65C=
ENST00000675906.1:c.*140C= ENSP00000502714.1:n.*140C=
ENST00000676231.1:c.585C= ENSP00000502249.1:p.Phe195=
ENST00000248553.6:c.555C= ENSP00000248553.6:p.Phe185=
ENST00000429938.1:c.51C= ENSP00000405285.1:p.Phe17=
ENST00000447574.1:c.*719C= ENSP00000414357.1:n.*719C=
NM_001540.3:c.555C= , LRG_248t1:c.555C= NP_001531.1:p.Phe185=
NM_001540.4:c.555C= NP_001531.1:p.Phe185=
NM_001540.5:c.555C= MANE Select NP_001531.1:p.Phe185=