Canonical Allele Identifier: CA2044300708
Gene: LYZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353301T= , CM000674.2:g.69353301T= GRCh38
NC_000012.11:g.69747081T= , CM000674.1:g.69747081T= GRCh37
NC_000012.10:g.68033348T= NCBI36
NG_008195.1:g.9948T= , LRG_768:g.9948T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*82T= MANE Select ENSP00000261267.2:n.*82T=
ENST00000261267.6:c.*82T= ENSP00000261267.2:n.*82T=
ENST00000549690.1:c.*36T= ENSP00000449898.1:n.*36T=
NM_000239.2:c.*82T= , LRG_768t1:c.*82T= NP_000230.1:n.*82T=
NM_000239.3:c.*82T= MANE Select NP_000230.1:n.*82T=