Canonical Allele Identifier: CA2044300851
Gene: LYZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353479T= , CM000674.2:g.69353479T= GRCh38
NC_000012.11:g.69747259T= , CM000674.1:g.69747259T= GRCh37
NC_000012.10:g.68033526T= NCBI36
NG_008195.1:g.10126T= , LRG_768:g.10126T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*260T= MANE Select ENSP00000261267.2:n.*260T=
ENST00000261267.6:c.*260T= ENSP00000261267.2:n.*260T=
ENST00000549690.1:c.*214T= ENSP00000449898.1:n.*214T=
NM_000239.2:c.*260T= , LRG_768t1:c.*260T= NP_000230.1:n.*260T=
NM_000239.3:c.*260T= MANE Select NP_000230.1:n.*260T=