Canonical Allele Identifier: CA1604334207

Gene: SQSTM1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.179833830A= , CM000667.2:g.179833830A=	GRCh38
NC_000005.9:g.179260830A= , CM000667.1:g.179260830A=	GRCh37
NC_000005.8:g.179193436A=	NCBI36
NG_011342.1:g.32443A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389805.9:c.1165+48A= MANE Select	ENSP00000374455.4:n.1165+48A=
ENST00000360718.5:c.913+48A=	ENSP00000353944.5:n.913+48A=
ENST00000389805.8:c.1165+48A=	ENSP00000374455.4:n.1165+48A=
ENST00000510187.5:c.950+603A=	ENSP00000424477.1:n.950+603A=
NM_001142298.1:c.913+48A=	NP_001135770.1:n.913+48A=
NM_001142299.1:c.913+48A=	NP_001135771.1:n.913+48A=
NM_003900.4:c.1165+48A=	NP_003891.1:n.1165+48A=
XM_017010010.1:c.913+48A=	XP_016865499.1:n.913+48A=
NM_003900.5:c.1165+48A= MANE Select	NP_003891.1:n.1165+48A=
NM_001142298.2:c.913+48A=	NP_001135770.1:n.913+48A=
NM_001142299.2:c.913+48A=	NP_001135771.1:n.913+48A=