Canonical Allele Identifier: CA2334219

Gene: LYZL4

Linked Data

• dbSNP Id: rs755162347
• ExAC: 3:42448478 G / A
• gnomAD v2: 3-42448478-G-A
• gnomAD v4: 3-42406986-G-A
• MyVariant Identifiers: chr3:g.42448478G>A (hg19) ; chr3:g.42406986G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.42406986G>A , CM000665.2:g.42406986G>A	GRCh38
NC_000003.11:g.42448478G>A , CM000665.1:g.42448478G>A	GRCh37
NC_000003.10:g.42423482G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000287748.8:c.152C>T MANE Select	ENSP00000287748.3:p.Ala51Val
ENST00000287748.7:c.152C>T	ENSP00000287748.3:p.Ala51Val
ENST00000441172.1:c.152C>T	ENSP00000387897.1:p.Ala51Val
ENST00000470991.1:n.182C>T
NM_001304386.1:c.152C>T	NP_001291315.1:p.Ala51Val
NM_144634.3:c.152C>T	NP_653235.1:p.Ala51Val
XM_011533355.1:c.152C>T	XP_011531657.1:p.Ala51Val
XM_011533355.3:c.152C>T	XP_011531657.1:p.Ala51Val
XM_017005706.1:c.152C>T	XP_016861195.1:p.Ala51Val
XM_024453345.1:c.152C>T	XP_024309113.1:p.Ala51Val
NM_144634.4:c.152C>T MANE Select	NP_653235.1:p.Ala51Val
NM_001304386.2:c.152C>T	NP_001291315.1:p.Ala51Val