Canonical Allele Identifier: CA2666464435
Gene: LMOD3 HGNC NCBI

Linked Data

gnomAD v4: 3-69119483-TTGG-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69119484_69119486del , CM000665.2:g.69119484_69119486del GRCh38
NC_000003.11:g.69168635_69168637del , CM000665.1:g.69168635_69168637del GRCh37
NC_000003.10:g.69251325_69251327del NCBI36
NG_041828.1:g.8110_8112del

Transcript Alleles

HGVS Amino-acid Change
ENST00000420581.7:c.869_871del MANE Select ENSP00000414670.3:p.Ala290_Asn291delinsAsp
ENST00000420581.6:c.869_871del ENSP00000414670.2:p.Ala290_Asn291delinsAsp
ENST00000475434.1:c.869_871del ENSP00000418645.1:p.Ala290_Asn291delinsAsp
ENST00000489031.5:c.869_871del ENSP00000417210.1:p.Ala290_Asn291delinsAsp
NM_001304418.1:c.869_871del NP_001291347.1:p.Ala290_Asn291delinsAsp
NM_198271.4:c.869_871del NP_938012.2:p.Ala290_Asn291delinsAsp
NM_001304418.3:c.869_871del NP_001291347.1:p.Ala290_Asn291delinsAsp
NM_198271.5:c.869_871del MANE Select NP_938012.2:p.Ala290_Asn291delinsAsp
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