Canonical Allele Identifier: CA948901511
Gene: LYZ HGNC NCBI

Linked Data

dbSNP Id: rs2120837267

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353511del , CM000674.2:g.69353511del GRCh38
NC_000012.11:g.69747291del , CM000674.1:g.69747291del GRCh37
NC_000012.10:g.68033558del NCBI36
NG_008195.1:g.10158del , LRG_768:g.10158del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*292del MANE Select ENSP00000261267.2:n.*292del
ENST00000261267.6:c.*292del ENSP00000261267.2:n.*292del
NM_000239.2:c.*292del , LRG_768t1:c.*292del NP_000230.1:n.*292del
NM_000239.3:c.*292del MANE Select NP_000230.1:n.*292del