Canonical Allele Identifier: CA10118796
Community Standard Title: NM_006767.4(LZTR1):c.1261-2A>G
Gene: LZTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20993660A>G , CM000684.2:g.20993660A>G GRCh38
NC_000022.10:g.21347949A>G , CM000684.1:g.21347949A>G GRCh37
NC_000022.9:g.19677949A>G NCBI36
NG_034193.1:g.16392A>G

Transcript Alleles

HGVS Amino-acid Change
NM_006767.4:c.1261-2A>G MANE Select NP_006758.2:n.1261-2A>G
ENST00000646124.2:c.1261-2A>G MANE Select ENSP00000496779.1:n.1261-2A>G
NM_006767.3:c.1261-2A>G NP_006758.2:n.1261-2A>G
ENST00000215739.12:c.1261-2A>G ENSP00000215739.8:n.1261-2A>G
ENST00000479606.5:n.1407-2A>G
ENST00000492480.1:n.310-2A>G
ENST00000495142.6:n.606-2A>G
ENST00000642151.1:c.1092-2A>G
ENST00000643578.1:n.1283-2A>G
ENST00000643710.1:n.122-2A>G
ENST00000646506.1:n.840-2A>G
ENST00000700578.1:c.1261-2A>G ENSP00000515073.1:n.1261-2A>G