Canonical Allele Identifier: CA2676888068

Gene: SQSTM1

Linked Data

• gnomAD v4: 5-179823854-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.179823855del , CM000667.2:g.179823855del	GRCh38
NC_000005.9:g.179250855del , CM000667.1:g.179250855del	GRCh37
NC_000005.8:g.179183461del	NCBI36
NG_011342.1:g.22468del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389805.9:c.302-3del MANE Select	ENSP00000374455.4:n.302-3del
ENST00000360718.5:c.50-3del	ENSP00000353944.5:n.50-3del
ENST00000389805.8:c.302-3del	ENSP00000374455.4:n.302-3del
ENST00000422245.5:c.50-3del	ENSP00000394534.1:n.50-3del
ENST00000453046.5:c.*237-3del	ENSP00000405061.1:n.*237-3del
ENST00000464493.5:n.197-3del
ENST00000481335.5:n.452-3del
ENST00000485412.1:n.291del
ENST00000504627.1:c.371-3del	ENSP00000425957.1:n.371-3del
ENST00000508284.5:c.*24-3del	ENSP00000424195.1:n.*24-3del
ENST00000510187.5:c.302-3del	ENSP00000424477.1:n.302-3del
ENST00000514093.5:c.50-3del	ENSP00000427308.1:n.50-3del
NM_001142298.1:c.50-3del	NP_001135770.1:n.50-3del
NM_001142299.1:c.50-3del	NP_001135771.1:n.50-3del
NM_003900.4:c.302-3del	NP_003891.1:n.302-3del
XM_017010010.1:c.50-3del	XP_016865499.1:n.50-3del
NM_003900.5:c.302-3del MANE Select	NP_003891.1:n.302-3del
NM_001142298.2:c.50-3del	NP_001135770.1:n.50-3del
NM_001142299.2:c.50-3del	NP_001135771.1:n.50-3del