Canonical Allele Identifier: CA1604334232

Gene: SQSTM1

Linked Data

• dbSNP Id: rs1758367815

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.179833867_179833868del , CM000667.2:g.179833867_179833868del	GRCh38
NC_000005.9:g.179260867_179260868del , CM000667.1:g.179260867_179260868del	GRCh37
NC_000005.8:g.179193473_179193474del	NCBI36
NG_011342.1:g.32480_32481del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389805.9:c.1165+85_1165+86del MANE Select	ENSP00000374455.4:n.1165+85_1165+86del
ENST00000360718.5:c.913+85_913+86del	ENSP00000353944.5:n.913+85_913+86del
ENST00000389805.8:c.1165+85_1165+86del	ENSP00000374455.4:n.1165+85_1165+86del
ENST00000510187.5:c.950+640_950+641del	ENSP00000424477.1:n.950+640_950+641del
NM_001142298.1:c.913+85_913+86del	NP_001135770.1:n.913+85_913+86del
NM_001142299.1:c.913+85_913+86del	NP_001135771.1:n.913+85_913+86del
NM_003900.4:c.1165+85_1165+86del	NP_003891.1:n.1165+85_1165+86del
XM_017010010.1:c.913+85_913+86del	XP_016865499.1:n.913+85_913+86del
NM_003900.5:c.1165+85_1165+86del MANE Select	NP_003891.1:n.1165+85_1165+86del
NM_001142298.2:c.913+85_913+86del	NP_001135770.1:n.913+85_913+86del
NM_001142299.2:c.913+85_913+86del	NP_001135771.1:n.913+85_913+86del