Canonical Allele Identifier: CA1718331541
Gene: HSPB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.76304111G= , CM000669.2:g.76304111G= GRCh38
NC_000007.13:g.75933428G= , CM000669.1:g.75933428G= GRCh37
NC_000007.12:g.75771364G= NCBI36
NG_008995.1:g.6554G= , LRG_248:g.6554G=

Transcript Alleles

HGVS Amino-acid change
ENST00000248553.7:c.556G= MANE Select ENSP00000248553.6:p.Glu186=
ENST00000674547.1:c.*147G= ENSP00000502461.1:n.*147G=
ENST00000674638.1:c.*77G= ENSP00000502651.1:n.*77G=
ENST00000674650.1:c.*66G= ENSP00000501628.1:n.*66G=
ENST00000674965.1:c.*212G= ENSP00000501765.1:n.*212G=
ENST00000675134.1:c.535G= ENSP00000501831.1:p.Glu179=
ENST00000675226.1:c.*66G= ENSP00000502510.1:n.*66G=
ENST00000675417.1:n.907G=
ENST00000675538.1:c.*66G= ENSP00000502495.1:n.*66G=
ENST00000675906.1:c.*141G= ENSP00000502714.1:n.*141G=
ENST00000676231.1:c.586G= ENSP00000502249.1:p.Glu196=
ENST00000248553.6:c.556G= ENSP00000248553.6:p.Glu186=
ENST00000429938.1:c.52G= ENSP00000405285.1:p.Glu18=
ENST00000447574.1:c.*720G= ENSP00000414357.1:n.*720G=
NM_001540.3:c.556G= , LRG_248t1:c.556G= NP_001531.1:p.Glu186=
NM_001540.4:c.556G= NP_001531.1:p.Glu186=
NM_001540.5:c.556G= MANE Select NP_001531.1:p.Glu186=