Canonical Allele Identifier: CA362443828

Gene: SQSTM1

Linked Data

• COSMIC: COSM4414008
• MyVariant Identifiers: chr5:g.179250983A>T (hg19) ; chr5:g.179823983A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.179823983A>T , CM000667.2:g.179823983A>T	GRCh38
NC_000005.9:g.179250983A>T , CM000667.1:g.179250983A>T	GRCh37
NC_000005.8:g.179183589A>T	NCBI36
NG_011342.1:g.22596A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389805.9:c.427A>T MANE Select	ENSP00000374455.4:p.Ser143Cys
ENST00000360718.5:c.175A>T	ENSP00000353944.5:p.Ser59Cys
ENST00000389805.8:c.427A>T	ENSP00000374455.4:p.Ser143Cys
ENST00000422245.5:c.175A>T	ENSP00000394534.1:p.Ser59Cys
ENST00000464493.5:n.322A>T
ENST00000466342.1:n.126A>T
ENST00000485412.1:n.419A>T
ENST00000504627.1:c.496A>T	ENSP00000425957.1:p.Ser166Cys
ENST00000508284.5:c.*149A>T	ENSP00000424195.1:n.*149A>T
ENST00000510187.5:c.427A>T	ENSP00000424477.1:p.Ser143Cys
ENST00000514093.5:c.175A>T	ENSP00000427308.1:p.Ser59Cys
NM_001142298.1:c.175A>T	NP_001135770.1:p.Ser59Cys
NM_001142299.1:c.175A>T	NP_001135771.1:p.Ser59Cys
NM_003900.4:c.427A>T	NP_003891.1:p.Ser143Cys
XM_017010010.1:c.175A>T	XP_016865499.1:p.Ser59Cys
NM_003900.5:c.427A>T MANE Select	NP_003891.1:p.Ser143Cys
NM_001142298.2:c.175A>T	NP_001135770.1:p.Ser59Cys
NM_001142299.2:c.175A>T	NP_001135771.1:p.Ser59Cys