Canonical Allele Identifier: CA2044300749
Gene: LYZ HGNC NCBI

Linked Data

dbSNP Id: rs1874886614

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353354del , CM000674.2:g.69353354del GRCh38
NC_000012.11:g.69747134del , CM000674.1:g.69747134del GRCh37
NC_000012.10:g.68033401del NCBI36
NG_008195.1:g.10001del , LRG_768:g.10001del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*135del MANE Select ENSP00000261267.2:n.*135del
ENST00000261267.6:c.*135del ENSP00000261267.2:n.*135del
ENST00000549690.1:c.*89del ENSP00000449898.1:n.*89del
NM_000239.2:c.*135del , LRG_768t1:c.*135del NP_000230.1:n.*135del
NM_000239.3:c.*135del MANE Select NP_000230.1:n.*135del