Canonical Allele Identifier: CA352336978

Gene: LYZL4

Linked Data

• dbSNP Id: rs1334560223
• gnomAD v2: 3-42448374-C-T
• gnomAD v3: 3-42406882-C-T
• gnomAD v4: 3-42406882-C-T
• MyVariant Identifiers: chr3:g.42448374C>T (hg19) ; chr3:g.42406882C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.42406882C>T , CM000665.2:g.42406882C>T	GRCh38
NC_000003.11:g.42448374C>T , CM000665.1:g.42448374C>T	GRCh37
NC_000003.10:g.42423378C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000287748.8:c.256G>A MANE Select	ENSP00000287748.3:p.Asp86Asn
ENST00000287748.7:c.256G>A	ENSP00000287748.3:p.Asp86Asn
ENST00000441172.1:c.256G>A	ENSP00000387897.1:p.Asp86Asn
ENST00000470991.1:n.286G>A
NM_001304386.1:c.256G>A	NP_001291315.1:p.Asp86Asn
NM_144634.3:c.256G>A	NP_653235.1:p.Asp86Asn
XM_011533355.1:c.256G>A	XP_011531657.1:p.Asp86Asn
XM_011533355.3:c.256G>A	XP_011531657.1:p.Asp86Asn
XM_017005706.1:c.256G>A	XP_016861195.1:p.Asp86Asn
XM_024453345.1:c.256G>A	XP_024309113.1:p.Asp86Asn
NM_144634.4:c.256G>A MANE Select	NP_653235.1:p.Asp86Asn
NM_001304386.2:c.256G>A	NP_001291315.1:p.Asp86Asn