Canonical Allele Identifier: CA1604334192

Gene: SQSTM1

Linked Data

• dbSNP Id: rs1758363882
• gnomAD v4: 5-179833810-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.179833810A>G , CM000667.2:g.179833810A>G	GRCh38
NC_000005.9:g.179260810A>G , CM000667.1:g.179260810A>G	GRCh37
NC_000005.8:g.179193416A>G	NCBI36
NG_011342.1:g.32423A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389805.9:c.1165+28A>G MANE Select	ENSP00000374455.4:n.1165+28A>G
ENST00000360718.5:c.913+28A>G	ENSP00000353944.5:n.913+28A>G
ENST00000389805.8:c.1165+28A>G	ENSP00000374455.4:n.1165+28A>G
ENST00000510187.5:c.950+583A>G	ENSP00000424477.1:n.950+583A>G
NM_001142298.1:c.913+28A>G	NP_001135770.1:n.913+28A>G
NM_001142299.1:c.913+28A>G	NP_001135771.1:n.913+28A>G
NM_003900.4:c.1165+28A>G	NP_003891.1:n.1165+28A>G
XM_017010010.1:c.913+28A>G	XP_016865499.1:n.913+28A>G
NM_003900.5:c.1165+28A>G MANE Select	NP_003891.1:n.1165+28A>G
NM_001142298.2:c.913+28A>G	NP_001135770.1:n.913+28A>G
NM_001142299.2:c.913+28A>G	NP_001135771.1:n.913+28A>G