Canonical Allele Identifier: CA352337358
Gene: LYZL4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.42406980A>T , CM000665.2:g.42406980A>T GRCh38
NC_000003.11:g.42448472A>T , CM000665.1:g.42448472A>T GRCh37
NC_000003.10:g.42423476A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000287748.8:c.158T>A MANE Select ENSP00000287748.3:p.Phe53Tyr
ENST00000287748.7:c.158T>A ENSP00000287748.3:p.Phe53Tyr
ENST00000441172.1:c.158T>A ENSP00000387897.1:p.Phe53Tyr
ENST00000470991.1:n.188T>A
NM_001304386.1:c.158T>A NP_001291315.1:p.Phe53Tyr
NM_144634.3:c.158T>A NP_653235.1:p.Phe53Tyr
XM_011533355.1:c.158T>A XP_011531657.1:p.Phe53Tyr
XM_011533355.3:c.158T>A XP_011531657.1:p.Phe53Tyr
XM_017005706.1:c.158T>A XP_016861195.1:p.Phe53Tyr
XM_024453345.1:c.158T>A XP_024309113.1:p.Phe53Tyr
NM_144634.4:c.158T>A MANE Select NP_653235.1:p.Phe53Tyr
NM_001304386.2:c.158T>A NP_001291315.1:p.Phe53Tyr