Canonical Allele Identifier: CA2044298697
Gene: LYZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69350194T= , CM000674.2:g.69350194T= GRCh38
NC_000012.11:g.69743974T= , CM000674.1:g.69743974T= GRCh37
NC_000012.10:g.68030241T= NCBI36
NG_008195.1:g.6841T= , LRG_768:g.6841T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.223T= MANE Select ENSP00000261267.2:p.Phe75=
ENST00000261267.6:c.223T= ENSP00000261267.2:p.Phe75=
ENST00000548839.1:c.223T= ENSP00000449969.1:p.Phe75=
ENST00000549690.1:c.223T= ENSP00000449898.1:p.Phe75=
NM_000239.2:c.223T= , LRG_768t1:c.223T= NP_000230.1:p.Phe75=
NM_000239.3:c.223T= MANE Select NP_000230.1:p.Phe75=