Canonical Allele Identifier: CA1604334215

Gene: SQSTM1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.179833839_179833842delinsCCCT , CM000667.2:g.179833839_179833842delinsCCCT	GRCh38
NC_000005.9:g.179260839_179260842delinsCCCT , CM000667.1:g.179260839_179260842delinsCCCT	GRCh37
NC_000005.8:g.179193445_179193448delinsCCCT	NCBI36
NG_011342.1:g.32452_32455delinsCCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389805.9:c.1165+57_1165+60delinsCCCT MANE Select	ENSP00000374455.4:n.1165+57_1165+60delinsCCCT
ENST00000360718.5:c.913+57_913+60delinsCCCT	ENSP00000353944.5:n.913+57_913+60delinsCCCT
ENST00000389805.8:c.1165+57_1165+60delinsCCCT	ENSP00000374455.4:n.1165+57_1165+60delinsCCCT
ENST00000510187.5:c.950+612_950+615delinsCCCT	ENSP00000424477.1:n.950+612_950+615delinsCCCT
NM_001142298.1:c.913+57_913+60delinsCCCT	NP_001135770.1:n.913+57_913+60delinsCCCT
NM_001142299.1:c.913+57_913+60delinsCCCT	NP_001135771.1:n.913+57_913+60delinsCCCT
NM_003900.4:c.1165+57_1165+60delinsCCCT	NP_003891.1:n.1165+57_1165+60delinsCCCT
XM_017010010.1:c.913+57_913+60delinsCCCT	XP_016865499.1:n.913+57_913+60delinsCCCT
NM_003900.5:c.1165+57_1165+60delinsCCCT MANE Select	NP_003891.1:n.1165+57_1165+60delinsCCCT
NM_001142298.2:c.913+57_913+60delinsCCCT	NP_001135770.1:n.913+57_913+60delinsCCCT
NM_001142299.2:c.913+57_913+60delinsCCCT	NP_001135771.1:n.913+57_913+60delinsCCCT