Canonical Allele Identifier: CA1360330765
Gene: LYZL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.42406981A= , CM000665.2:g.42406981A= GRCh38
NC_000003.11:g.42448473A= , CM000665.1:g.42448473A= GRCh37
NC_000003.10:g.42423477A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000287748.8:c.157T= MANE Select ENSP00000287748.3:p.Phe53=
ENST00000287748.7:c.157T= ENSP00000287748.3:p.Phe53=
ENST00000441172.1:c.157T= ENSP00000387897.1:p.Phe53=
ENST00000470991.1:n.187T=
NM_001304386.1:c.157T= NP_001291315.1:p.Phe53=
NM_144634.3:c.157T= NP_653235.1:p.Phe53=
XM_011533355.1:c.157T= XP_011531657.1:p.Phe53=
XM_011533355.3:c.157T= XP_011531657.1:p.Phe53=
XM_017005706.1:c.157T= XP_016861195.1:p.Phe53=
XM_024453345.1:c.157T= XP_024309113.1:p.Phe53=
NM_144634.4:c.157T= MANE Select NP_653235.1:p.Phe53=
NM_001304386.2:c.157T= NP_001291315.1:p.Phe53=