Canonical Allele Identifier: CA2044301178
Gene: LYZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353626T= , CM000674.2:g.69353626T= GRCh38
NC_000012.11:g.69747406T= , CM000674.1:g.69747406T= GRCh37
NC_000012.10:g.68033673T= NCBI36
NG_008195.1:g.10273T= , LRG_768:g.10273T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*407T= MANE Select ENSP00000261267.2:n.*407T=
ENST00000261267.6:c.*407T= ENSP00000261267.2:n.*407T=
NM_000239.2:c.*407T= , LRG_768t1:c.*407T= NP_000230.1:n.*407T=
NM_000239.3:c.*407T= MANE Select NP_000230.1:n.*407T=