Canonical Allele Identifier: CA2044300642
Gene: LYZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353253T= , CM000674.2:g.69353253T= GRCh38
NC_000012.11:g.69747033T= , CM000674.1:g.69747033T= GRCh37
NC_000012.10:g.68033300T= NCBI36
NG_008195.1:g.9900T= , LRG_768:g.9900T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*34T= MANE Select ENSP00000261267.2:n.*34T=
ENST00000261267.6:c.*34T= ENSP00000261267.2:n.*34T=
ENST00000549690.1:c.402T= ENSP00000449898.1:p.Ser134=
NM_000239.2:c.*34T= , LRG_768t1:c.*34T= NP_000230.1:n.*34T=
NM_000239.3:c.*34T= MANE Select NP_000230.1:n.*34T=