Canonical Allele Identifier: CA1604334216

Gene: SQSTM1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.179833843_179833845delinsCCT , CM000667.2:g.179833843_179833845delinsCCT	GRCh38
NC_000005.9:g.179260843_179260845delinsCCT , CM000667.1:g.179260843_179260845delinsCCT	GRCh37
NC_000005.8:g.179193449_179193451delinsCCT	NCBI36
NG_011342.1:g.32456_32458delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389805.9:c.1165+61_1165+63delinsCCT MANE Select	ENSP00000374455.4:n.1165+61_1165+63delinsCCT
ENST00000360718.5:c.913+61_913+63delinsCCT	ENSP00000353944.5:n.913+61_913+63delinsCCT
ENST00000389805.8:c.1165+61_1165+63delinsCCT	ENSP00000374455.4:n.1165+61_1165+63delinsCCT
ENST00000510187.5:c.950+616_950+618delinsCCT	ENSP00000424477.1:n.950+616_950+618delinsCCT
NM_001142298.1:c.913+61_913+63delinsCCT	NP_001135770.1:n.913+61_913+63delinsCCT
NM_001142299.1:c.913+61_913+63delinsCCT	NP_001135771.1:n.913+61_913+63delinsCCT
NM_003900.4:c.1165+61_1165+63delinsCCT	NP_003891.1:n.1165+61_1165+63delinsCCT
XM_017010010.1:c.913+61_913+63delinsCCT	XP_016865499.1:n.913+61_913+63delinsCCT
NM_003900.5:c.1165+61_1165+63delinsCCT MANE Select	NP_003891.1:n.1165+61_1165+63delinsCCT
NM_001142298.2:c.913+61_913+63delinsCCT	NP_001135770.1:n.913+61_913+63delinsCCT
NM_001142299.2:c.913+61_913+63delinsCCT	NP_001135771.1:n.913+61_913+63delinsCCT