Canonical Allele Identifier: CA10119089
Community Standard Title: NM_006767.4(LZTR1):c.1855C>T (p.Arg619Cys)
Gene: LZTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20994939C>T , CM000684.2:g.20994939C>T GRCh38
NC_000022.10:g.21349228C>T , CM000684.1:g.21349228C>T GRCh37
NC_000022.9:g.19679228C>T NCBI36
NG_034193.1:g.17671C>T

Transcript Alleles

HGVS Amino-acid Change
NM_006767.4:c.1855C>T MANE Select NP_006758.2:p.Arg619Cys
ENST00000646124.2:c.1855C>T MANE Select ENSP00000496779.1:p.Arg619Cys
NM_006767.3:c.1855C>T NP_006758.2:p.Arg619Cys
ENST00000215739.12:c.1855C>T ENSP00000215739.8:p.Arg619Cys
ENST00000415354.6:c.167C>T ENSP00000393765.2:p.Ala56Val
ENST00000415817.2:c.167C>T
ENST00000439171.5:c.137C>T
ENST00000452988.5:c.34C>T ENSP00000408789.1:p.Arg12Cys
ENST00000464807.1:n.116C>T
ENST00000479606.5:n.2001C>T
ENST00000491432.5:n.276C>T
ENST00000495142.5:n.471C>T
ENST00000495142.6:n.1488C>T
ENST00000642151.1:c.1686C>T
ENST00000643578.1:n.1877C>T
ENST00000643710.1:n.716C>T
ENST00000646506.1:n.1722C>T
ENST00000700578.1:c.1855C>T ENSP00000515073.1:p.Arg619Cys