Canonical Allele Identifier: CA433356050
Gene: LYZL4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.42448372G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.42406880G>A , CM000665.2:g.42406880G>A GRCh38
NC_000003.11:g.42448372G>A , CM000665.1:g.42448372G>A GRCh37
NC_000003.10:g.42423376G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000287748.8:c.258C>T MANE Select ENSP00000287748.3:p.Asp86=
ENST00000287748.7:c.258C>T ENSP00000287748.3:p.Asp86=
ENST00000441172.1:c.258C>T ENSP00000387897.1:p.Asp86=
ENST00000470991.1:n.288C>T
NM_001304386.1:c.258C>T NP_001291315.1:p.Asp86=
NM_144634.3:c.258C>T NP_653235.1:p.Asp86=
XM_011533355.1:c.258C>T XP_011531657.1:p.Asp86=
XM_011533355.3:c.258C>T XP_011531657.1:p.Asp86=
XM_017005706.1:c.258C>T XP_016861195.1:p.Asp86=
XM_024453345.1:c.258C>T XP_024309113.1:p.Asp86=
NM_144634.4:c.258C>T MANE Select NP_653235.1:p.Asp86=
NM_001304386.2:c.258C>T NP_001291315.1:p.Asp86=