Canonical Allele Identifier: CA10118326
Community Standard Title: NM_006767.4(LZTR1):c.263+5G>T
Gene: LZTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20983094G>T , CM000684.2:g.20983094G>T GRCh38
NC_000022.10:g.21337383G>T , CM000684.1:g.21337383G>T GRCh37
NC_000022.9:g.19667383G>T NCBI36
NG_034193.1:g.5826G>T

Transcript Alleles

HGVS Amino-acid Change
NM_006767.4:c.263+5G>T MANE Select NP_006758.2:n.263+5G>T
ENST00000646124.2:c.263+5G>T MANE Select ENSP00000496779.1:n.263+5G>T
NM_006767.3:c.263+5G>T NP_006758.2:n.263+5G>T
ENST00000215739.12:c.263+5G>T ENSP00000215739.8:n.263+5G>T
ENST00000414985.5:c.263+5G>T ENSP00000397247.1:n.263+5G>T
ENST00000443265.5:c.268+5G>T ENSP00000406466.1:n.268+5G>T
ENST00000479606.5:n.409+5G>T
ENST00000493460.1:n.338+5G>T
ENST00000493460.2:n.338+5G>T
ENST00000642151.1:c.146G>T
ENST00000644435.1:c.169+5G>T
ENST00000645935.1:c.263+5G>T ENSP00000493479.1:n.263+5G>T
ENST00000700578.1:c.263+5G>T ENSP00000515073.1:n.263+5G>T