Canonical Allele Identifier: CA352337009

Gene: LYZL4

Linked Data

• dbSNP Id: rs1455428359
• gnomAD v3: 3-42406889-C-A
• gnomAD v4: 3-42406889-C-A
• MyVariant Identifiers: chr3:g.42448381C>A (hg19) ; chr3:g.42406889C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.42406889C>A , CM000665.2:g.42406889C>A	GRCh38
NC_000003.11:g.42448381C>A , CM000665.1:g.42448381C>A	GRCh37
NC_000003.10:g.42423385C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287748.8:c.249G>T MANE Select	ENSP00000287748.3:p.Trp83Cys
ENST00000287748.7:c.249G>T	ENSP00000287748.3:p.Trp83Cys
ENST00000441172.1:c.249G>T	ENSP00000387897.1:p.Trp83Cys
ENST00000470991.1:n.279G>T
NM_001304386.1:c.249G>T	NP_001291315.1:p.Trp83Cys
NM_144634.3:c.249G>T	NP_653235.1:p.Trp83Cys
XM_011533355.1:c.249G>T	XP_011531657.1:p.Trp83Cys
XM_011533355.3:c.249G>T	XP_011531657.1:p.Trp83Cys
XM_017005706.1:c.249G>T	XP_016861195.1:p.Trp83Cys
XM_024453345.1:c.249G>T	XP_024309113.1:p.Trp83Cys
NM_144634.4:c.249G>T MANE Select	NP_653235.1:p.Trp83Cys
NM_001304386.2:c.249G>T	NP_001291315.1:p.Trp83Cys