Canonical Allele Identifier: CA410778806
Community Standard Title: NM_006767.4(LZTR1):c.1942G>T (p.Gly648Cys)
Gene: LZTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20995026G>T , CM000684.2:g.20995026G>T GRCh38
NC_000022.10:g.21349315G>T , CM000684.1:g.21349315G>T GRCh37
NC_000022.9:g.19679315G>T NCBI36
NG_034193.1:g.17758G>T

Transcript Alleles

HGVS Amino-acid Change
NM_006767.4:c.1942G>T MANE Select NP_006758.2:p.Gly648Cys
ENST00000646124.2:c.1942G>T MANE Select ENSP00000496779.1:p.Gly648Cys
NM_006767.3:c.1942G>T NP_006758.2:p.Gly648Cys
ENST00000215739.12:c.1942G>T ENSP00000215739.8:p.Gly648Cys
ENST00000415354.6:c.254G>T ENSP00000393765.2:p.Trp85Leu
ENST00000415817.2:c.254G>T
ENST00000439171.5:c.224G>T
ENST00000452988.5:c.121G>T ENSP00000408789.1:p.Gly41Ter
ENST00000464807.1:n.203G>T
ENST00000479606.5:n.2088G>T
ENST00000491432.5:n.363G>T
ENST00000495142.5:n.558G>T
ENST00000495142.6:n.1575G>T
ENST00000642151.1:c.1773G>T
ENST00000643578.1:n.1964G>T
ENST00000643710.1:n.803G>T
ENST00000646506.1:n.1809G>T
ENST00000700578.1:c.1942G>T ENSP00000515073.1:p.Gly648Cys