Canonical Allele Identifier: CA410779656
Community Standard Title: NM_006767.4(LZTR1):c.416A>G (p.Asp139Gly)
Gene: LZTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20988025A>G , CM000684.2:g.20988025A>G GRCh38
NC_000022.10:g.21342314A>G , CM000684.1:g.21342314A>G GRCh37
NC_000022.9:g.19672314A>G NCBI36
NG_034193.1:g.10757A>G

Transcript Alleles

HGVS Amino-acid Change
NM_006767.4:c.416A>G MANE Select NP_006758.2:p.Asp139Gly
ENST00000646124.2:c.416A>G MANE Select ENSP00000496779.1:p.Asp139Gly
NM_006767.3:c.416A>G NP_006758.2:p.Asp139Gly
ENST00000215739.12:c.416A>G ENSP00000215739.8:p.Asp139Gly
ENST00000414985.5:c.336A>G ENSP00000397247.1:p.Gly112=
ENST00000443265.5:c.*115A>G ENSP00000406466.1:n.*115A>G
ENST00000479606.5:n.562A>G
ENST00000480895.1:n.112A>G
ENST00000642151.1:c.247A>G
ENST00000644435.1:c.322A>G
ENST00000645935.1:c.359A>G ENSP00000493479.1:p.Asp120Gly
ENST00000700578.1:c.416A>G ENSP00000515073.1:p.Asp139Gly