Canonical Allele Identifier: CA2044301255
Gene: LYZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353659T= , CM000674.2:g.69353659T= GRCh38
NC_000012.11:g.69747439T= , CM000674.1:g.69747439T= GRCh37
NC_000012.10:g.68033706T= NCBI36
NG_008195.1:g.10306T= , LRG_768:g.10306T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*440T= MANE Select ENSP00000261267.2:n.*440T=
ENST00000261267.6:c.*440T= ENSP00000261267.2:n.*440T=
NM_000239.2:c.*440T= , LRG_768t1:c.*440T= NP_000230.1:n.*440T=
NM_000239.3:c.*440T= MANE Select NP_000230.1:n.*440T=