Canonical Allele Identifier: CA2578916979

Gene: HSPB1

Linked Data

• gnomAD v4: 7-76303900-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303901del , CM000669.2:g.76303901del	GRCh38
NC_000007.13:g.75933218del , CM000669.1:g.75933218del	GRCh37
NC_000007.12:g.75771154del	NCBI36
NG_008995.1:g.6344del , LRG_248:g.6344del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.428+36del MANE Select	ENSP00000248553.6:n.428+36del
ENST00000674547.1:c.*19+13del	ENSP00000502461.1:n.*19+13del
ENST00000674638.1:c.423+36del	ENSP00000502651.1:n.423+36del
ENST00000674650.1:c.365-83del	ENSP00000501628.1:n.365-83del
ENST00000674965.1:c.*84+36del	ENSP00000501765.1:n.*84+36del
ENST00000675134.1:c.407+57del	ENSP00000501831.1:n.407+57del
ENST00000675226.1:c.427+36del	ENSP00000502510.1:n.427+36del
ENST00000675417.1:n.697del
ENST00000675538.1:c.463+36del	ENSP00000502495.1:n.463+36del
ENST00000675906.1:c.*13+19del	ENSP00000502714.1:n.*13+19del
ENST00000676231.1:c.458+36del	ENSP00000502249.1:n.458+36del
ENST00000248553.6:c.428+36del	ENSP00000248553.6:n.428+36del
ENST00000429938.1:c.-77+36del	ENSP00000405285.1:n.-77+36del
ENST00000447574.1:c.*592+36del	ENSP00000414357.1:n.*592+36del
NM_001540.3:c.428+36del , LRG_248t1:c.428+36del	NP_001531.1:n.428+36del
NM_001540.4:c.428+36del	NP_001531.1:n.428+36del
NM_001540.5:c.428+36del MANE Select	NP_001531.1:n.428+36del