Canonical Allele Identifier: CA2683408094
Gene: HSPB1 HGNC NCBI

Linked Data

gnomAD v4: 7-76303725-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.76303725G>T , CM000669.2:g.76303725G>T GRCh38
NC_000007.13:g.75933042G>T , CM000669.1:g.75933042G>T GRCh37
NC_000007.12:g.75770978G>T NCBI36
NG_008995.1:g.6168G>T , LRG_248:g.6168G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248553.7:c.365-77G>T MANE Select ENSP00000248553.6:n.365-77G>T
ENST00000674547.1:c.365-77G>T ENSP00000502461.1:n.365-77G>T
ENST00000674638.1:c.365-82G>T ENSP00000502651.1:n.365-82G>T
ENST00000674650.1:c.365-259G>T ENSP00000501628.1:n.365-259G>T
ENST00000674965.1:c.365-52G>T ENSP00000501765.1:n.365-52G>T
ENST00000675134.1:c.365-77G>T ENSP00000501831.1:n.365-77G>T
ENST00000675226.1:c.369-82G>T ENSP00000502510.1:n.369-82G>T
ENST00000675417.1:n.521G>T
ENST00000675538.1:c.400-77G>T ENSP00000502495.1:n.400-77G>T
ENST00000675733.1:n.405-37G>T
ENST00000675906.1:c.365-77G>T ENSP00000502714.1:n.365-77G>T
ENST00000676195.1:n.80+69G>T
ENST00000676231.1:c.392G>T ENSP00000502249.1:p.Gly131Val
ENST00000248553.6:c.365-77G>T ENSP00000248553.6:n.365-77G>T
ENST00000429938.1:c.-143G>T ENSP00000405285.1:n.-143G>T
ENST00000447574.1:c.*452G>T ENSP00000414357.1:n.*452G>T
NM_001540.3:c.365-77G>T , LRG_248t1:c.365-77G>T NP_001531.1:n.365-77G>T
NM_001540.4:c.365-77G>T NP_001531.1:n.365-77G>T
NM_001540.5:c.365-77G>T MANE Select NP_001531.1:n.365-77G>T