Canonical Allele Identifier: CA3260261931
Community Standard Title: NM_006767.4(LZTR1):c.486del (p.Trp162Ter)
Gene: LZTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20988095del , CM000684.2:g.20988095del GRCh38
NC_000022.10:g.21342384del , CM000684.1:g.21342384del GRCh37
NC_000022.9:g.19672384del NCBI36
NG_034193.1:g.10827del

Transcript Alleles

HGVS Amino-acid Change
NM_006767.4:c.486del MANE Select NP_006758.2:p.Trp162Ter
ENST00000646124.2:c.486del MANE Select ENSP00000496779.1:p.Trp162Ter
NM_006767.3:c.486del NP_006758.2:p.Trp162Ter
ENST00000215739.12:c.486del ENSP00000215739.8:p.Trp162Ter
ENST00000414985.5:c.*52del ENSP00000397247.1:n.*52del
ENST00000443265.5:c.*185del ENSP00000406466.1:n.*185del
ENST00000479606.5:n.632del
ENST00000480895.1:n.182del
ENST00000642151.1:c.317del
ENST00000644435.1:c.392del
ENST00000645935.1:c.429del ENSP00000493479.1:p.Trp143Ter
ENST00000646506.1:n.65del
ENST00000700578.1:c.486del ENSP00000515073.1:p.Trp162Ter