Canonical Allele Identifier: CA10119195
Community Standard Title: NM_006767.4(LZTR1):c.2002G>T (p.Asp668Tyr)
Gene: LZTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20995805G>T , CM000684.2:g.20995805G>T GRCh38
NC_000022.10:g.21350094G>T , CM000684.1:g.21350094G>T GRCh37
NC_000022.9:g.19680094G>T NCBI36
NG_034193.1:g.18537G>T

Transcript Alleles

HGVS Amino-acid Change
NM_006767.4:c.2002G>T MANE Select NP_006758.2:p.Asp668Tyr
ENST00000646124.2:c.2002G>T MANE Select ENSP00000496779.1:p.Asp668Tyr
NM_006767.3:c.2002G>T NP_006758.2:p.Asp668Tyr
ENST00000215739.12:c.2002G>T ENSP00000215739.8:p.Asp668Tyr
ENST00000415354.6:c.431G>T ENSP00000393765.2:n.431G>T
ENST00000415817.2:c.431G>T
ENST00000439171.5:c.401G>T
ENST00000452988.5:c.164G>T ENSP00000408789.1:p.Ter55Leu
ENST00000463909.1:n.717G>T
ENST00000479606.5:n.2148G>T
ENST00000491432.5:n.423G>T
ENST00000495142.5:n.618G>T
ENST00000495142.6:n.2354G>T
ENST00000498649.1:n.18G>T
ENST00000642151.1:c.1833G>T
ENST00000643578.1:n.2024G>T
ENST00000643710.1:n.863G>T
ENST00000646506.1:n.1869G>T
ENST00000700578.1:c.2002G>T ENSP00000515073.1:p.Asp668Tyr