Canonical Allele Identifier: CA10119098
Community Standard Title: NM_006767.4(LZTR1):c.1889G>A (p.Arg630Gln)
Gene: LZTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20994973G>A , CM000684.2:g.20994973G>A GRCh38
NC_000022.10:g.21349262G>A , CM000684.1:g.21349262G>A GRCh37
NC_000022.9:g.19679262G>A NCBI36
NG_034193.1:g.17705G>A

Transcript Alleles

HGVS Amino-acid Change
NM_006767.4:c.1889G>A MANE Select NP_006758.2:p.Arg630Gln
ENST00000646124.2:c.1889G>A MANE Select ENSP00000496779.1:p.Arg630Gln
NM_006767.3:c.1889G>A NP_006758.2:p.Arg630Gln
ENST00000215739.12:c.1889G>A ENSP00000215739.8:p.Arg630Gln
ENST00000415354.6:c.201G>A ENSP00000393765.2:p.Ala67=
ENST00000415817.2:c.201G>A
ENST00000439171.5:c.171G>A
ENST00000452988.5:c.68G>A ENSP00000408789.1:p.Arg23Gln
ENST00000464807.1:n.150G>A
ENST00000479606.5:n.2035G>A
ENST00000491432.5:n.310G>A
ENST00000495142.5:n.505G>A
ENST00000495142.6:n.1522G>A
ENST00000642151.1:c.1720G>A
ENST00000643578.1:n.1911G>A
ENST00000643710.1:n.750G>A
ENST00000646506.1:n.1756G>A
ENST00000700578.1:c.1889G>A ENSP00000515073.1:p.Arg630Gln