Canonical Allele Identifier: CA1604328656

Gene: SQSTM1

Linked Data

• dbSNP Id: rs369958794

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.179823829C>G , CM000667.2:g.179823829C>G	GRCh38
NC_000005.9:g.179250829C>G , CM000667.1:g.179250829C>G	GRCh37
NC_000005.8:g.179183435C>G	NCBI36
NG_011342.1:g.22442C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389805.9:c.302-29C>G MANE Select	ENSP00000374455.4:n.302-29C>G
ENST00000360718.5:c.50-29C>G	ENSP00000353944.5:n.50-29C>G
ENST00000389805.8:c.302-29C>G	ENSP00000374455.4:n.302-29C>G
ENST00000422245.5:c.50-29C>G	ENSP00000394534.1:n.50-29C>G
ENST00000453046.5:c.*237-29C>G	ENSP00000405061.1:n.*237-29C>G
ENST00000464493.5:n.197-29C>G
ENST00000481335.5:n.452-29C>G
ENST00000485412.1:n.265C>G
ENST00000504627.1:c.371-29C>G	ENSP00000425957.1:n.371-29C>G
ENST00000508284.5:c.*24-29C>G	ENSP00000424195.1:n.*24-29C>G
ENST00000510187.5:c.302-29C>G	ENSP00000424477.1:n.302-29C>G
ENST00000514093.5:c.50-29C>G	ENSP00000427308.1:n.50-29C>G
NM_001142298.1:c.50-29C>G	NP_001135770.1:n.50-29C>G
NM_001142299.1:c.50-29C>G	NP_001135771.1:n.50-29C>G
NM_003900.4:c.302-29C>G	NP_003891.1:n.302-29C>G
XM_017010010.1:c.50-29C>G	XP_016865499.1:n.50-29C>G
NM_003900.5:c.302-29C>G MANE Select	NP_003891.1:n.302-29C>G
NM_001142298.2:c.50-29C>G	NP_001135770.1:n.50-29C>G
NM_001142299.2:c.50-29C>G	NP_001135771.1:n.50-29C>G