Canonical Allele Identifier: CA10118519
Community Standard Title: NM_006767.4(LZTR1):c.594-3C>T
Gene: LZTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20989622C>T , CM000684.2:g.20989622C>T GRCh38
NC_000022.10:g.21343911C>T , CM000684.1:g.21343911C>T GRCh37
NC_000022.9:g.19673911C>T NCBI36
NG_034193.1:g.12354C>T

Transcript Alleles

HGVS Amino-acid Change
NM_006767.4:c.594-3C>T MANE Select NP_006758.2:n.594-3C>T
ENST00000646124.2:c.594-3C>T MANE Select ENSP00000496779.1:n.594-3C>T
NM_006767.3:c.594-3C>T NP_006758.2:n.594-3C>T
ENST00000215739.12:c.594-3C>T ENSP00000215739.8:n.594-3C>T
ENST00000414985.5:c.*160-3C>T ENSP00000397247.1:n.*160-3C>T
ENST00000443265.5:c.*293-3C>T ENSP00000406466.1:n.*293-3C>T
ENST00000479606.5:n.740-3C>T
ENST00000480895.1:n.290-3C>T
ENST00000642151.1:c.425-3C>T
ENST00000644435.1:c.416-3C>T
ENST00000646506.1:n.173-3C>T
ENST00000700578.1:c.594-3C>T ENSP00000515073.1:n.594-3C>T