Canonical Allele Identifier: CA2044301001
Gene: LYZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353499T= , CM000674.2:g.69353499T= GRCh38
NC_000012.11:g.69747279T= , CM000674.1:g.69747279T= GRCh37
NC_000012.10:g.68033546T= NCBI36
NG_008195.1:g.10146T= , LRG_768:g.10146T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*280T= MANE Select ENSP00000261267.2:n.*280T=
ENST00000261267.6:c.*280T= ENSP00000261267.2:n.*280T=
NM_000239.2:c.*280T= , LRG_768t1:c.*280T= NP_000230.1:n.*280T=
NM_000239.3:c.*280T= MANE Select NP_000230.1:n.*280T=