Canonical Allele Identifier: CA2581524712
Gene: SQSTM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.179833528T>A , CM000667.2:g.179833528T>A GRCh38
NC_000005.9:g.179260528T>A , CM000667.1:g.179260528T>A GRCh37
NC_000005.8:g.179193134T>A NCBI36
NG_011342.1:g.32141T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000389805.9:c.970-59T>A MANE Select ENSP00000374455.4:n.970-59T>A
ENST00000360718.5:c.718-59T>A ENSP00000353944.5:n.718-59T>A
ENST00000389805.8:c.970-59T>A ENSP00000374455.4:n.970-59T>A
ENST00000510187.5:c.950+301T>A ENSP00000424477.1:n.950+301T>A
NM_001142298.1:c.718-59T>A NP_001135770.1:n.718-59T>A
NM_001142299.1:c.718-59T>A NP_001135771.1:n.718-59T>A
NM_003900.4:c.970-59T>A NP_003891.1:n.970-59T>A
XM_017010010.1:c.718-59T>A XP_016865499.1:n.718-59T>A
NM_003900.5:c.970-59T>A MANE Select NP_003891.1:n.970-59T>A
NM_001142298.2:c.718-59T>A NP_001135770.1:n.718-59T>A
NM_001142299.2:c.718-59T>A NP_001135771.1:n.718-59T>A