Canonical Allele Identifier: CA1604328755

Gene: SQSTM1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.179823990G= , CM000667.2:g.179823990G=	GRCh38
NC_000005.9:g.179250990G= , CM000667.1:g.179250990G=	GRCh37
NC_000005.8:g.179183596G=	NCBI36
NG_011342.1:g.22603G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389805.9:c.434G= MANE Select	ENSP00000374455.4:p.Cys145=
ENST00000360718.5:c.182G=	ENSP00000353944.5:p.Cys61=
ENST00000389805.8:c.434G=	ENSP00000374455.4:p.Cys145=
ENST00000422245.5:c.182G=	ENSP00000394534.1:p.Cys61=
ENST00000464493.5:n.329G=
ENST00000466342.1:n.133G=
ENST00000485412.1:n.426G=
ENST00000504627.1:c.503G=	ENSP00000425957.1:p.Cys168=
ENST00000508284.5:c.*156G=	ENSP00000424195.1:n.*156G=
ENST00000510187.5:c.434G=	ENSP00000424477.1:p.Cys145=
ENST00000514093.5:c.182G=	ENSP00000427308.1:p.Cys61=
NM_001142298.1:c.182G=	NP_001135770.1:p.Cys61=
NM_001142299.1:c.182G=	NP_001135771.1:p.Cys61=
NM_003900.4:c.434G=	NP_003891.1:p.Cys145=
XM_017010010.1:c.182G=	XP_016865499.1:p.Cys61=
NM_003900.5:c.434G= MANE Select	NP_003891.1:p.Cys145=
NM_001142298.2:c.182G=	NP_001135770.1:p.Cys61=
NM_001142299.2:c.182G=	NP_001135771.1:p.Cys61=