Canonical Allele Identifier: CA3600532

Gene: SQSTM1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.179824069C>G , CM000667.2:g.179824069C>G	GRCh38
NC_000005.9:g.179251069C>G , CM000667.1:g.179251069C>G	GRCh37
NC_000005.8:g.179183675C>G	NCBI36
NG_011342.1:g.22682C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_003900.5:c.513C>G MANE Select	NP_003891.1:p.Pro171=
ENST00000389805.9:c.513C>G MANE Select	ENSP00000374455.4:p.Pro171=
NM_001142298.1:c.261C>G	NP_001135770.1:p.Pro87=
NM_001142298.2:c.261C>G	NP_001135770.1:p.Pro87=
NM_001142299.1:c.261C>G	NP_001135771.1:p.Pro87=
NM_001142299.2:c.261C>G	NP_001135771.1:p.Pro87=
NM_003900.4:c.513C>G	NP_003891.1:p.Pro171=
ENST00000360718.5:c.261C>G	ENSP00000353944.5:p.Pro87=
ENST00000389805.8:c.513C>G	ENSP00000374455.4:p.Pro171=
ENST00000422245.5:c.261C>G	ENSP00000394534.1:p.Pro87=
ENST00000464493.5:n.408C>G
ENST00000466342.1:n.212C>G
ENST00000485412.1:n.505C>G
ENST00000508284.5:c.*235C>G	ENSP00000424195.1:n.*235C>G
ENST00000510187.5:c.513C>G	ENSP00000424477.1:p.Pro171=
ENST00000514093.5:c.261C>G	ENSP00000427308.1:p.Pro87=
XM_017010010.1:c.261C>G	XP_016865499.1:p.Pro87=