Canonical Allele Identifier: CA2578916958
Gene: HSPB1 HGNC NCBI

Linked Data

gnomAD v4: 7-76303728-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.76303728G>C , CM000669.2:g.76303728G>C GRCh38
NC_000007.13:g.75933045G>C , CM000669.1:g.75933045G>C GRCh37
NC_000007.12:g.75770981G>C NCBI36
NG_008995.1:g.6171G>C , LRG_248:g.6171G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000248553.7:c.365-74G>C MANE Select ENSP00000248553.6:n.365-74G>C
ENST00000674547.1:c.365-74G>C ENSP00000502461.1:n.365-74G>C
ENST00000674638.1:c.365-79G>C ENSP00000502651.1:n.365-79G>C
ENST00000674650.1:c.365-256G>C ENSP00000501628.1:n.365-256G>C
ENST00000674965.1:c.365-49G>C ENSP00000501765.1:n.365-49G>C
ENST00000675134.1:c.365-74G>C ENSP00000501831.1:n.365-74G>C
ENST00000675226.1:c.369-79G>C ENSP00000502510.1:n.369-79G>C
ENST00000675417.1:n.524G>C
ENST00000675538.1:c.400-74G>C ENSP00000502495.1:n.400-74G>C
ENST00000675733.1:n.405-34G>C
ENST00000675906.1:c.365-74G>C ENSP00000502714.1:n.365-74G>C
ENST00000676195.1:n.80+72G>C
ENST00000676231.1:c.394+1G>C ENSP00000502249.1:n.394+1G>C
ENST00000248553.6:c.365-74G>C ENSP00000248553.6:n.365-74G>C
ENST00000429938.1:c.-141+1G>C ENSP00000405285.1:n.-141+1G>C
ENST00000447574.1:c.*455G>C ENSP00000414357.1:n.*455G>C
NM_001540.3:c.365-74G>C , LRG_248t1:c.365-74G>C NP_001531.1:n.365-74G>C
NM_001540.4:c.365-74G>C NP_001531.1:n.365-74G>C
NM_001540.5:c.365-74G>C MANE Select NP_001531.1:n.365-74G>C