Canonical Allele Identifier: CA2488869
Gene: LMOD3 HGNC NCBI

Linked Data

dbSNP Id: rs757277832
ExAC: 3:69168454 A / AT
gnomAD v2: 3-69168454-A-AT
gnomAD v3: 3-69119303-A-AT
gnomAD v4: 3-69119303-A-AT
MyVariant Identifiers: chr3:g.69168454_69168455insT (hg19) chr3:g.69119303_69119304insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69119304dup , CM000665.2:g.69119304dup GRCh38
NC_000003.11:g.69168455dup , CM000665.1:g.69168455dup GRCh37
NC_000003.10:g.69251145dup NCBI36
NG_041828.1:g.8292dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000420581.7:c.1051dup MANE Select ENSP00000414670.3:p.Met351AsnfsTer7
ENST00000420581.6:c.1051dup ENSP00000414670.2:p.Met351AsnfsTer7
ENST00000475434.1:c.1051dup ENSP00000418645.1:p.Met351AsnfsTer7
ENST00000489031.5:c.1051dup ENSP00000417210.1:p.Met351AsnfsTer7
NM_001304418.1:c.1051dup NP_001291347.1:p.Met351AsnfsTer7
NM_198271.4:c.1051dup NP_938012.2:p.Met351AsnfsTer7
NM_001304418.3:c.1051dup NP_001291347.1:p.Met351AsnfsTer7
NM_198271.5:c.1051dup MANE Select NP_938012.2:p.Met351AsnfsTer7
Search 100 bp 5'
Search 100 bp 3'