Canonical Allele Identifier: CA2683408907

Gene: HSPB1

Linked Data

• gnomAD v4: 7-76303897-GTGGCGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76303898_76303903del , CM000669.2:g.76303898_76303903del	GRCh38
NC_000007.13:g.75933215_75933220del , CM000669.1:g.75933215_75933220del	GRCh37
NC_000007.12:g.75771151_75771156del	NCBI36
NG_008995.1:g.6341_6346del , LRG_248:g.6341_6346del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.428+33_428+38del MANE Select	ENSP00000248553.6:n.428+33_428+38del
ENST00000674547.1:c.*19+10_*19+15del	ENSP00000502461.1:n.*19+10_*19+15del
ENST00000674638.1:c.423+33_423+38del	ENSP00000502651.1:n.423+33_423+38del
ENST00000674650.1:c.365-86_365-81del	ENSP00000501628.1:n.365-86_365-81del
ENST00000674965.1:c.*84+33_*84+38del	ENSP00000501765.1:n.*84+33_*84+38del
ENST00000675134.1:c.407+54_407+59del	ENSP00000501831.1:n.407+54_407+59del
ENST00000675226.1:c.427+33_427+38del	ENSP00000502510.1:n.427+33_427+38del
ENST00000675417.1:n.694_699del
ENST00000675538.1:c.463+33_463+38del	ENSP00000502495.1:n.463+33_463+38del
ENST00000675906.1:c.*13+16_*13+21del	ENSP00000502714.1:n.*13+16_*13+21del
ENST00000676231.1:c.458+33_458+38del	ENSP00000502249.1:n.458+33_458+38del
ENST00000248553.6:c.428+33_428+38del	ENSP00000248553.6:n.428+33_428+38del
ENST00000429938.1:c.-77+33_-77+38del	ENSP00000405285.1:n.-77+33_-77+38del
ENST00000447574.1:c.*592+33_*592+38del	ENSP00000414357.1:n.*592+33_*592+38del
NM_001540.3:c.428+33_428+38del , LRG_248t1:c.428+33_428+38del	NP_001531.1:n.428+33_428+38del
NM_001540.4:c.428+33_428+38del	NP_001531.1:n.428+33_428+38del
NM_001540.5:c.428+33_428+38del MANE Select	NP_001531.1:n.428+33_428+38del