Canonical Allele Identifier: CA501021
Community Standard Title: NM_006767.4(LZTR1):c.2090G>A (p.Arg697Gln)
Gene: LZTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20995983G>A , CM000684.2:g.20995983G>A GRCh38
NC_000022.10:g.21350272G>A , CM000684.1:g.21350272G>A GRCh37
NC_000022.9:g.19680272G>A NCBI36
NG_034193.1:g.18715G>A

Transcript Alleles

HGVS Amino-acid Change
NM_006767.4:c.2090G>A MANE Select NP_006758.2:p.Arg697Gln
ENST00000646124.2:c.2090G>A MANE Select ENSP00000496779.1:p.Arg697Gln
NM_006767.3:c.2090G>A NP_006758.2:p.Arg697Gln
ENST00000215739.12:c.2090G>A ENSP00000215739.8:p.Arg697Gln
ENST00000415354.6:c.519G>A ENSP00000393765.2:n.519G>A
ENST00000415817.2:c.519G>A
ENST00000439171.5:c.489G>A
ENST00000452988.5:c.252G>A ENSP00000408789.1:n.252G>A
ENST00000463909.1:n.805G>A
ENST00000479606.5:n.2236G>A
ENST00000491432.5:n.511G>A
ENST00000495142.5:n.706G>A
ENST00000495142.6:n.2442G>A
ENST00000498649.1:n.106G>A
ENST00000642151.1:c.1921G>A
ENST00000643578.1:n.2112G>A
ENST00000643710.1:n.951G>A
ENST00000646506.1:n.1957G>A
ENST00000700578.1:c.2090G>A ENSP00000515073.1:p.Arg697Gln