Canonical Allele Identifier: CA367765589

Gene: HSPB1

Linked Data

• gnomAD v4: 7-76303863-C-G
• MyVariant Identifiers: chr7:g.75933180C>G (hg19) ; chr7:g.76303863C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303863C>G , CM000669.2:g.76303863C>G	GRCh38
NC_000007.13:g.75933180C>G , CM000669.1:g.75933180C>G	GRCh37
NC_000007.12:g.75771116C>G	NCBI36
NG_008995.1:g.6306C>G , LRG_248:g.6306C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000248553.7:c.426C>G MANE Select	ENSP00000248553.6:p.Tyr142Ter
ENST00000674547.1:c.426C>G	ENSP00000502461.1:p.Tyr142Ter
ENST00000674638.1:c.421C>G	ENSP00000502651.1:p.His141Asp
ENST00000674650.1:c.365-121C>G	ENSP00000501628.1:n.365-121C>G
ENST00000674965.1:c.*82C>G	ENSP00000501765.1:n.*82C>G
ENST00000675134.1:c.407+19C>G	ENSP00000501831.1:n.407+19C>G
ENST00000675226.1:c.425C>G	ENSP00000502510.1:p.Thr142Arg
ENST00000675417.1:n.659C>G
ENST00000675538.1:c.461C>G	ENSP00000502495.1:p.Thr154Arg
ENST00000675906.1:c.426C>G	ENSP00000502714.1:p.Tyr142Ter
ENST00000676195.1:n.142C>G
ENST00000676231.1:c.456C>G	ENSP00000502249.1:p.Tyr152Ter
ENST00000248553.6:c.426C>G	ENSP00000248553.6:p.Tyr142Ter
ENST00000429938.1:c.-79C>G	ENSP00000405285.1:n.-79C>G
ENST00000447574.1:c.*590C>G	ENSP00000414357.1:n.*590C>G
NM_001540.3:c.426C>G , LRG_248t1:c.426C>G	NP_001531.1:p.Tyr142Ter
NM_001540.4:c.426C>G	NP_001531.1:p.Tyr142Ter
NM_001540.5:c.426C>G MANE Select	NP_001531.1:p.Tyr142Ter