Canonical Allele Identifier: CA410779194
Community Standard Title: NM_006767.4(LZTR1):c.2076T>G (p.Phe692Leu)
Gene: LZTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20995969T>G , CM000684.2:g.20995969T>G GRCh38
NC_000022.10:g.21350258T>G , CM000684.1:g.21350258T>G GRCh37
NC_000022.9:g.19680258T>G NCBI36
NG_034193.1:g.18701T>G

Transcript Alleles

HGVS Amino-acid Change
NM_006767.4:c.2076T>G MANE Select NP_006758.2:p.Phe692Leu
ENST00000646124.2:c.2076T>G MANE Select ENSP00000496779.1:p.Phe692Leu
NM_006767.3:c.2076T>G NP_006758.2:p.Phe692Leu
ENST00000215739.12:c.2076T>G ENSP00000215739.8:p.Phe692Leu
ENST00000415354.6:c.505T>G ENSP00000393765.2:n.505T>G
ENST00000415817.2:c.505T>G
ENST00000439171.5:c.475T>G
ENST00000452988.5:c.238T>G ENSP00000408789.1:n.238T>G
ENST00000463909.1:n.791T>G
ENST00000479606.5:n.2222T>G
ENST00000491432.5:n.497T>G
ENST00000495142.5:n.692T>G
ENST00000495142.6:n.2428T>G
ENST00000498649.1:n.92T>G
ENST00000642151.1:c.1907T>G
ENST00000643578.1:n.2098T>G
ENST00000643710.1:n.937T>G
ENST00000646506.1:n.1943T>G
ENST00000700578.1:c.2076T>G ENSP00000515073.1:p.Phe692Leu