Canonical Allele Identifier: CA1604321519
Gene: SQSTM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.179811261C= , CM000667.2:g.179811261C= GRCh38
NC_000005.9:g.179238261C= , CM000667.1:g.179238261C= GRCh37
NC_000005.8:g.179170867C= NCBI36
NG_011342.1:g.9874C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000506042.5:n.195-313C=
ENST00000506690.1:n.1105-313C=
ENST00000514093.5:c.-156-313C= ENSP00000427308.1:n.-156-313C=
NM_001142298.1:c.-156-313C= NP_001135770.1:n.-156-313C=
NM_001142299.1:c.-156-313C= NP_001135771.1:n.-156-313C=
XM_011534683.1:c.500-313C= XP_011532985.1:n.500-313C=
XM_011534684.1:c.500-313C= XP_011532986.1:n.500-313C=
NM_001142298.2:c.-156-313C= NP_001135770.1:n.-156-313C=
NM_001142299.2:c.-156-313C= NP_001135771.1:n.-156-313C=