Canonical Allele Identifier: CA1604334210

Gene: SQSTM1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.179833832_179833833delinsCA , CM000667.2:g.179833832_179833833delinsCA	GRCh38
NC_000005.9:g.179260832_179260833delinsCA , CM000667.1:g.179260832_179260833delinsCA	GRCh37
NC_000005.8:g.179193438_179193439delinsCA	NCBI36
NG_011342.1:g.32445_32446delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389805.9:c.1165+50_1165+51delinsCA MANE Select	ENSP00000374455.4:n.1165+50_1165+51delinsCA
ENST00000360718.5:c.913+50_913+51delinsCA	ENSP00000353944.5:n.913+50_913+51delinsCA
ENST00000389805.8:c.1165+50_1165+51delinsCA	ENSP00000374455.4:n.1165+50_1165+51delinsCA
ENST00000510187.5:c.950+605_950+606delinsCA	ENSP00000424477.1:n.950+605_950+606delinsCA
NM_001142298.1:c.913+50_913+51delinsCA	NP_001135770.1:n.913+50_913+51delinsCA
NM_001142299.1:c.913+50_913+51delinsCA	NP_001135771.1:n.913+50_913+51delinsCA
NM_003900.4:c.1165+50_1165+51delinsCA	NP_003891.1:n.1165+50_1165+51delinsCA
XM_017010010.1:c.913+50_913+51delinsCA	XP_016865499.1:n.913+50_913+51delinsCA
NM_003900.5:c.1165+50_1165+51delinsCA MANE Select	NP_003891.1:n.1165+50_1165+51delinsCA
NM_001142298.2:c.913+50_913+51delinsCA	NP_001135770.1:n.913+50_913+51delinsCA
NM_001142299.2:c.913+50_913+51delinsCA	NP_001135771.1:n.913+50_913+51delinsCA