Canonical Allele Identifier: CA808343971
Gene: SQSTM1 HGNC NCBI

Linked Data

dbSNP Id: rs1340818287
MyVariant Identifiers: chr5:g.179260833del (hg19) chr5:g.179833833del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.179833833del , CM000667.2:g.179833833del GRCh38
NC_000005.9:g.179260833del , CM000667.1:g.179260833del GRCh37
NC_000005.8:g.179193439del NCBI36
NG_011342.1:g.32446del

Transcript Alleles

HGVS Amino-acid Change
ENST00000389805.9:c.1165+51del MANE Select ENSP00000374455.4:n.1165+51del
ENST00000360718.5:c.913+51del ENSP00000353944.5:n.913+51del
ENST00000389805.8:c.1165+51del ENSP00000374455.4:n.1165+51del
ENST00000510187.5:c.950+606del ENSP00000424477.1:n.950+606del
NM_001142298.1:c.913+51del NP_001135770.1:n.913+51del
NM_001142299.1:c.913+51del NP_001135771.1:n.913+51del
NM_003900.4:c.1165+51del NP_003891.1:n.1165+51del
XM_017010010.1:c.913+51del XP_016865499.1:n.913+51del
NM_003900.5:c.1165+51del MANE Select NP_003891.1:n.1165+51del
NM_001142298.2:c.913+51del NP_001135770.1:n.913+51del
NM_001142299.2:c.913+51del NP_001135771.1:n.913+51del
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