Canonical Allele Identifier: CA410780262
Community Standard Title: NM_006767.4(LZTR1):c.594-2A>G
Gene: LZTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20989623A>G , CM000684.2:g.20989623A>G GRCh38
NC_000022.10:g.21343912A>G , CM000684.1:g.21343912A>G GRCh37
NC_000022.9:g.19673912A>G NCBI36
NG_034193.1:g.12355A>G

Transcript Alleles

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