Canonical Allele Identifier: CA2044301098
Gene: LYZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353553A= , CM000674.2:g.69353553A= GRCh38
NC_000012.11:g.69747333A= , CM000674.1:g.69747333A= GRCh37
NC_000012.10:g.68033600A= NCBI36
NG_008195.1:g.10200A= , LRG_768:g.10200A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*334A= MANE Select ENSP00000261267.2:n.*334A=
ENST00000261267.6:c.*334A= ENSP00000261267.2:n.*334A=
NM_000239.2:c.*334A= , LRG_768t1:c.*334A= NP_000230.1:n.*334A=
NM_000239.3:c.*334A= MANE Select NP_000230.1:n.*334A=