Canonical Allele Identifier: CA410777893
Community Standard Title: NM_006767.4(LZTR1):c.1702C>T (p.Gln568Ter)
Gene: LZTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20994644C>T , CM000684.2:g.20994644C>T GRCh38
NC_000022.10:g.21348933C>T , CM000684.1:g.21348933C>T GRCh37
NC_000022.9:g.19678933C>T NCBI36
NG_034193.1:g.17376C>T

Transcript Alleles

HGVS Amino-acid Change
NM_006767.4:c.1702C>T MANE Select NP_006758.2:p.Gln568Ter
ENST00000646124.2:c.1702C>T MANE Select ENSP00000496779.1:p.Gln568Ter
NM_006767.3:c.1702C>T NP_006758.2:p.Gln568Ter
ENST00000215739.12:c.1702C>T ENSP00000215739.8:p.Gln568Ter
ENST00000415354.6:c.44-30C>T ENSP00000393765.2:n.44-30C>T
ENST00000415817.2:c.59C>T
ENST00000479606.5:n.1848C>T
ENST00000491432.5:n.168C>T
ENST00000495142.5:n.318C>T
ENST00000495142.6:n.1335C>T
ENST00000642151.1:c.1533C>T
ENST00000643578.1:n.1724C>T
ENST00000643710.1:n.563C>T
ENST00000646506.1:n.1569C>T
ENST00000700578.1:c.1702C>T ENSP00000515073.1:p.Gln568Ter