Canonical Allele Identifier: CA1604334135

Gene: SQSTM1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.179833730G= , CM000667.2:g.179833730G=	GRCh38
NC_000005.9:g.179260730G= , CM000667.1:g.179260730G=	GRCh37
NC_000005.8:g.179193336G=	NCBI36
NG_011342.1:g.32343G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389805.9:c.1113G= MANE Select	ENSP00000374455.4:p.Gln371=
ENST00000360718.5:c.861G=	ENSP00000353944.5:p.Gln287=
ENST00000389805.8:c.1113G=	ENSP00000374455.4:p.Gln371=
ENST00000510187.5:c.950+503G=	ENSP00000424477.1:n.950+503G=
NM_001142298.1:c.861G=	NP_001135770.1:p.Gln287=
NM_001142299.1:c.861G=	NP_001135771.1:p.Gln287=
NM_003900.4:c.1113G=	NP_003891.1:p.Gln371=
XM_017010010.1:c.861G=	XP_016865499.1:p.Gln287=
NM_003900.5:c.1113G= MANE Select	NP_003891.1:p.Gln371=
NM_001142298.2:c.861G=	NP_001135770.1:p.Gln287=
NM_001142299.2:c.861G=	NP_001135771.1:p.Gln287=