Canonical Allele Identifier: CA206838
Gene: ASNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97864268del , CM000669.2:g.97864268del GRCh38
NC_000007.13:g.97493580del , CM000669.1:g.97493580del GRCh37
NC_000007.12:g.97331516del NCBI36
NG_033870.1:g.13275del
NG_033870.2:g.69295del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394308.8:c.478del MANE Select ENSP00000377845.3:p.Glu160LysfsTer8
ENST00000175506.8:c.478del ENSP00000175506.4:p.Glu160LysfsTer8
ENST00000394308.7:c.478del ENSP00000377845.3:p.Glu160LysfsTer8
ENST00000394309.7:c.478del ENSP00000377846.3:p.Glu160LysfsTer8
ENST00000422745.5:c.415del ENSP00000414901.1:p.Glu139LysfsTer8
ENST00000437628.5:c.229del ENSP00000414379.1:p.Glu77LysfsTer8
ENST00000437657.5:c.478del ENSP00000394242.1:p.Glu160LysfsTer?
ENST00000442734.5:c.478del ENSP00000400422.1:p.Glu160LysfsTer8
ENST00000444334.5:c.415del ENSP00000406994.1:p.Glu139LysfsTer8
ENST00000454046.5:c.478del ENSP00000401651.1:p.Glu160LysfsTer8
ENST00000455086.5:c.229del ENSP00000408472.1:p.Glu77LysfsTer8
ENST00000495255.1:n.506del
NM_001178075.1:c.415del NP_001171546.1:p.Glu139LysfsTer8
NM_001178076.1:c.229del NP_001171547.1:p.Glu77LysfsTer8
NM_001178077.1:c.229del NP_001171548.1:p.Glu77LysfsTer8
NM_001673.4:c.478del NP_001664.3:p.Glu160LysfsTer8
NM_133436.3:c.478del NP_597680.2:p.Glu160LysfsTer8
NM_183356.3:c.478del NP_899199.2:p.Glu160LysfsTer8
NM_001352496.1:c.478del NP_001339425.1:p.Glu160LysfsTer8
NR_147989.1:n.2107del
NM_001673.5:c.478del MANE Select NP_001664.3:p.Glu160LysfsTer8
NM_001178075.2:c.415del NP_001171546.1:p.Glu139LysfsTer8
NM_001178076.2:c.229del NP_001171547.1:p.Glu77LysfsTer8
NM_001352496.2:c.478del NP_001339425.1:p.Glu160LysfsTer8
NM_183356.4:c.478del NP_899199.2:p.Glu160LysfsTer8