Canonical Allele Identifier: CA2044301194
Gene: LYZ HGNC NCBI

Linked Data

dbSNP Id: rs2059270990

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353633del , CM000674.2:g.69353633del GRCh38
NC_000012.11:g.69747413del , CM000674.1:g.69747413del GRCh37
NC_000012.10:g.68033680del NCBI36
NG_008195.1:g.10280del , LRG_768:g.10280del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*414del MANE Select ENSP00000261267.2:n.*414del
ENST00000261267.6:c.*414del ENSP00000261267.2:n.*414del
NM_000239.2:c.*414del , LRG_768t1:c.*414del NP_000230.1:n.*414del
NM_000239.3:c.*414del MANE Select NP_000230.1:n.*414del