Canonical Allele Identifier: CA2676907724

Gene: SQSTM1

Linked Data

• gnomAD v4: 5-179833885-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.179833885C>T , CM000667.2:g.179833885C>T	GRCh38
NC_000005.9:g.179260885C>T , CM000667.1:g.179260885C>T	GRCh37
NC_000005.8:g.179193491C>T	NCBI36
NG_011342.1:g.32498C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389805.9:c.1165+103C>T MANE Select	ENSP00000374455.4:n.1165+103C>T
ENST00000360718.5:c.913+103C>T	ENSP00000353944.5:n.913+103C>T
ENST00000389805.8:c.1165+103C>T	ENSP00000374455.4:n.1165+103C>T
ENST00000510187.5:c.950+658C>T	ENSP00000424477.1:n.950+658C>T
NM_001142298.1:c.913+103C>T	NP_001135770.1:n.913+103C>T
NM_001142299.1:c.913+103C>T	NP_001135771.1:n.913+103C>T
NM_003900.4:c.1165+103C>T	NP_003891.1:n.1165+103C>T
XM_017010010.1:c.913+103C>T	XP_016865499.1:n.913+103C>T
NM_003900.5:c.1165+103C>T MANE Select	NP_003891.1:n.1165+103C>T
NM_001142298.2:c.913+103C>T	NP_001135770.1:n.913+103C>T
NM_001142299.2:c.913+103C>T	NP_001135771.1:n.913+103C>T