Canonical Allele Identifier: CA10118278
Community Standard Title: NM_006767.4(LZTR1):c.59C>T (p.Ala20Val)
Gene: LZTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20982430C>T , CM000684.2:g.20982430C>T GRCh38
NC_000022.10:g.21336719C>T , CM000684.1:g.21336719C>T GRCh37
NC_000022.9:g.19666719C>T NCBI36
NG_034193.1:g.5162C>T

Transcript Alleles

HGVS Amino-acid Change
NM_006767.4:c.59C>T MANE Select NP_006758.2:p.Ala20Val
ENST00000646124.2:c.59C>T MANE Select ENSP00000496779.1:p.Ala20Val
NM_006767.3:c.59C>T NP_006758.2:p.Ala20Val
ENST00000215739.12:c.59C>T ENSP00000215739.8:p.Ala20Val
ENST00000414985.5:c.59C>T ENSP00000397247.1:p.Ala20Val
ENST00000443265.5:c.59C>T ENSP00000406466.1:p.Ala20Val
ENST00000479606.5:n.347-597C>T
ENST00000493460.1:n.134C>T
ENST00000493460.2:n.134C>T
ENST00000645935.1:c.59C>T ENSP00000493479.1:p.Ala20Val
ENST00000700578.1:c.59C>T ENSP00000515073.1:p.Ala20Val