Canonical Allele Identifier: CA2044301180
Gene: LYZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353629C= , CM000674.2:g.69353629C= GRCh38
NC_000012.11:g.69747409C= , CM000674.1:g.69747409C= GRCh37
NC_000012.10:g.68033676C= NCBI36
NG_008195.1:g.10276C= , LRG_768:g.10276C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*410C= MANE Select ENSP00000261267.2:n.*410C=
ENST00000261267.6:c.*410C= ENSP00000261267.2:n.*410C=
NM_000239.2:c.*410C= , LRG_768t1:c.*410C= NP_000230.1:n.*410C=
NM_000239.3:c.*410C= MANE Select NP_000230.1:n.*410C=