Canonical Allele Identifier: CA2044301128
Gene: LYZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353580C= , CM000674.2:g.69353580C= GRCh38
NC_000012.11:g.69747360C= , CM000674.1:g.69747360C= GRCh37
NC_000012.10:g.68033627C= NCBI36
NG_008195.1:g.10227C= , LRG_768:g.10227C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*361C= MANE Select ENSP00000261267.2:n.*361C=
ENST00000261267.6:c.*361C= ENSP00000261267.2:n.*361C=
NM_000239.2:c.*361C= , LRG_768t1:c.*361C= NP_000230.1:n.*361C=
NM_000239.3:c.*361C= MANE Select NP_000230.1:n.*361C=