Canonical Allele Identifier: CA1604328683

Gene: SQSTM1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.179823871C= , CM000667.2:g.179823871C=	GRCh38
NC_000005.9:g.179250871C= , CM000667.1:g.179250871C=	GRCh37
NC_000005.8:g.179183477C=	NCBI36
NG_011342.1:g.22484C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389805.9:c.315C= MANE Select	ENSP00000374455.4:p.Cys105=
ENST00000360718.5:c.63C=	ENSP00000353944.5:p.Cys21=
ENST00000389805.8:c.315C=	ENSP00000374455.4:p.Cys105=
ENST00000422245.5:c.63C=	ENSP00000394534.1:p.Cys21=
ENST00000453046.5:c.*250C=	ENSP00000405061.1:n.*250C=
ENST00000464493.5:n.210C=
ENST00000466342.1:n.14C=
ENST00000481335.5:n.465C=
ENST00000485412.1:n.307C=
ENST00000504627.1:c.384C=	ENSP00000425957.1:p.Cys128=
ENST00000508284.5:c.*37C=	ENSP00000424195.1:n.*37C=
ENST00000510187.5:c.315C=	ENSP00000424477.1:p.Cys105=
ENST00000514093.5:c.63C=	ENSP00000427308.1:p.Cys21=
NM_001142298.1:c.63C=	NP_001135770.1:p.Cys21=
NM_001142299.1:c.63C=	NP_001135771.1:p.Cys21=
NM_003900.4:c.315C=	NP_003891.1:p.Cys105=
XM_017010010.1:c.63C=	XP_016865499.1:p.Cys21=
NM_003900.5:c.315C= MANE Select	NP_003891.1:p.Cys105=
NM_001142298.2:c.63C=	NP_001135770.1:p.Cys21=
NM_001142299.2:c.63C=	NP_001135771.1:p.Cys21=