Canonical Allele Identifier: CA2044301102
Gene: LYZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353558G= , CM000674.2:g.69353558G= GRCh38
NC_000012.11:g.69747338G= , CM000674.1:g.69747338G= GRCh37
NC_000012.10:g.68033605G= NCBI36
NG_008195.1:g.10205G= , LRG_768:g.10205G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*339G= MANE Select ENSP00000261267.2:n.*339G=
ENST00000261267.6:c.*339G= ENSP00000261267.2:n.*339G=
NM_000239.2:c.*339G= , LRG_768t1:c.*339G= NP_000230.1:n.*339G=
NM_000239.3:c.*339G= MANE Select NP_000230.1:n.*339G=