Canonical Allele Identifier: CA362452801

Gene: SQSTM1

Linked Data

• ClinVar Variation Id: 2953215
• ClinVar RCV Id: RCV003810333
• MyVariant Identifiers: chr5:g.179260698T>G (hg19) ; chr5:g.179833698T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.179833698T>G , CM000667.2:g.179833698T>G	GRCh38
NC_000005.9:g.179260698T>G , CM000667.1:g.179260698T>G	GRCh37
NC_000005.8:g.179193304T>G	NCBI36
NG_011342.1:g.32311T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389805.9:c.1081T>G MANE Select	ENSP00000374455.4:p.Ser361Ala
ENST00000360718.5:c.829T>G	ENSP00000353944.5:p.Ser277Ala
ENST00000389805.8:c.1081T>G	ENSP00000374455.4:p.Ser361Ala
ENST00000510187.5:c.950+471T>G	ENSP00000424477.1:n.950+471T>G
NM_001142298.1:c.829T>G	NP_001135770.1:p.Ser277Ala
NM_001142299.1:c.829T>G	NP_001135771.1:p.Ser277Ala
NM_003900.4:c.1081T>G	NP_003891.1:p.Ser361Ala
XM_017010010.1:c.829T>G	XP_016865499.1:p.Ser277Ala
NM_003900.5:c.1081T>G MANE Select	NP_003891.1:p.Ser361Ala
NM_001142298.2:c.829T>G	NP_001135770.1:p.Ser277Ala
NM_001142299.2:c.829T>G	NP_001135771.1:p.Ser277Ala