Canonical Allele Identifier: CA410779888
Community Standard Title: NM_006767.4(LZTR1):c.485G>A (p.Trp162Ter)
Gene: LZTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20988094G>A , CM000684.2:g.20988094G>A GRCh38
NC_000022.10:g.21342383G>A , CM000684.1:g.21342383G>A GRCh37
NC_000022.9:g.19672383G>A NCBI36
NG_034193.1:g.10826G>A

Transcript Alleles

HGVS Amino-acid Change
NM_006767.4:c.485G>A MANE Select NP_006758.2:p.Trp162Ter
ENST00000646124.2:c.485G>A MANE Select ENSP00000496779.1:p.Trp162Ter
NM_006767.3:c.485G>A NP_006758.2:p.Trp162Ter
ENST00000215739.12:c.485G>A ENSP00000215739.8:p.Trp162Ter
ENST00000414985.5:c.*51G>A ENSP00000397247.1:n.*51G>A
ENST00000443265.5:c.*184G>A ENSP00000406466.1:n.*184G>A
ENST00000479606.5:n.631G>A
ENST00000480895.1:n.181G>A
ENST00000642151.1:c.316G>A
ENST00000644435.1:c.391G>A
ENST00000645935.1:c.428G>A ENSP00000493479.1:p.Trp143Ter
ENST00000646506.1:n.64G>A
ENST00000700578.1:c.485G>A ENSP00000515073.1:p.Trp162Ter