Canonical Allele Identifier: CA1103330314

Gene: HSPB1

Linked Data

• dbSNP Id: rs1488494832
• gnomAD v3: 7-76303791-T-A
• gnomAD v4: 7-76303791-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303791T>A , CM000669.2:g.76303791T>A	GRCh38
NC_000007.13:g.75933108T>A , CM000669.1:g.75933108T>A	GRCh37
NC_000007.12:g.75771044T>A	NCBI36
NG_008995.1:g.6234T>A , LRG_248:g.6234T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.365-11T>A MANE Select	ENSP00000248553.6:n.365-11T>A
ENST00000674547.1:c.365-11T>A	ENSP00000502461.1:n.365-11T>A
ENST00000674638.1:c.365-16T>A	ENSP00000502651.1:n.365-16T>A
ENST00000674650.1:c.365-193T>A	ENSP00000501628.1:n.365-193T>A
ENST00000674965.1:c.*10T>A	ENSP00000501765.1:n.*10T>A
ENST00000675134.1:c.365-11T>A	ENSP00000501831.1:n.365-11T>A
ENST00000675226.1:c.369-16T>A	ENSP00000502510.1:n.369-16T>A
ENST00000675417.1:n.587T>A
ENST00000675538.1:c.400-11T>A	ENSP00000502495.1:n.400-11T>A
ENST00000675733.1:n.434T>A
ENST00000675906.1:c.365-11T>A	ENSP00000502714.1:n.365-11T>A
ENST00000676195.1:n.81-11T>A
ENST00000676231.1:c.395-11T>A	ENSP00000502249.1:n.395-11T>A
ENST00000248553.6:c.365-11T>A	ENSP00000248553.6:n.365-11T>A
ENST00000429938.1:c.-140-11T>A	ENSP00000405285.1:n.-140-11T>A
ENST00000447574.1:c.*518T>A	ENSP00000414357.1:n.*518T>A
NM_001540.3:c.365-11T>A , LRG_248t1:c.365-11T>A	NP_001531.1:n.365-11T>A
NM_001540.4:c.365-11T>A	NP_001531.1:n.365-11T>A
NM_001540.5:c.365-11T>A MANE Select	NP_001531.1:n.365-11T>A