Canonical Allele Identifier: CA2578916955
Gene: HSPB1 HGNC NCBI

Linked Data

gnomAD v4: 7-76303720-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.76303720A>T , CM000669.2:g.76303720A>T GRCh38
NC_000007.13:g.75933037A>T , CM000669.1:g.75933037A>T GRCh37
NC_000007.12:g.75770973A>T NCBI36
NG_008995.1:g.6163A>T , LRG_248:g.6163A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248553.7:c.365-82A>T MANE Select ENSP00000248553.6:n.365-82A>T
ENST00000674547.1:c.365-82A>T ENSP00000502461.1:n.365-82A>T
ENST00000674638.1:c.365-87A>T ENSP00000502651.1:n.365-87A>T
ENST00000674650.1:c.365-264A>T ENSP00000501628.1:n.365-264A>T
ENST00000674965.1:c.365-57A>T ENSP00000501765.1:n.365-57A>T
ENST00000675134.1:c.365-82A>T ENSP00000501831.1:n.365-82A>T
ENST00000675226.1:c.369-87A>T ENSP00000502510.1:n.369-87A>T
ENST00000675417.1:n.516A>T
ENST00000675538.1:c.400-82A>T ENSP00000502495.1:n.400-82A>T
ENST00000675733.1:n.405-42A>T
ENST00000675906.1:c.365-82A>T ENSP00000502714.1:n.365-82A>T
ENST00000676195.1:n.80+64A>T
ENST00000676231.1:c.387A>T ENSP00000502249.1:p.Gln129His
ENST00000248553.6:c.365-82A>T ENSP00000248553.6:n.365-82A>T
ENST00000429938.1:c.-148A>T ENSP00000405285.1:n.-148A>T
ENST00000447574.1:c.*447A>T ENSP00000414357.1:n.*447A>T
NM_001540.3:c.365-82A>T , LRG_248t1:c.365-82A>T NP_001531.1:n.365-82A>T
NM_001540.4:c.365-82A>T NP_001531.1:n.365-82A>T
NM_001540.5:c.365-82A>T MANE Select NP_001531.1:n.365-82A>T