Canonical Allele Identifier: CA410779891
Community Standard Title: NM_006767.4(LZTR1):c.486G>A (p.Trp162Ter)
Gene: LZTR1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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