Canonical Allele Identifier: CA3600795

Gene: SQSTM1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.179833705G>A , CM000667.2:g.179833705G>A	GRCh38
NC_000005.9:g.179260705G>A , CM000667.1:g.179260705G>A	GRCh37
NC_000005.8:g.179193311G>A	NCBI36
NG_011342.1:g.32318G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003900.5:c.1088G>A MANE Select	NP_003891.1:p.Gly363Glu
ENST00000389805.9:c.1088G>A MANE Select	ENSP00000374455.4:p.Gly363Glu
NM_001142298.1:c.836G>A	NP_001135770.1:p.Gly279Glu
NM_001142298.2:c.836G>A	NP_001135770.1:p.Gly279Glu
NM_001142299.1:c.836G>A	NP_001135771.1:p.Gly279Glu
NM_001142299.2:c.836G>A	NP_001135771.1:p.Gly279Glu
NM_003900.4:c.1088G>A	NP_003891.1:p.Gly363Glu
ENST00000360718.5:c.836G>A	ENSP00000353944.5:p.Gly279Glu
ENST00000389805.8:c.1088G>A	ENSP00000374455.4:p.Gly363Glu
ENST00000510187.5:c.950+478G>A	ENSP00000424477.1:n.950+478G>A
XM_017010010.1:c.836G>A	XP_016865499.1:p.Gly279Glu