Canonical Allele Identifier: CA16040682
Gene: LAMC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 370298
ClinVar RCV Id: RCV000410161
dbSNP Id: rs1057516383

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183235663_183235666del , CM000663.2:g.183235663_183235666del GRCh38
NC_000001.10:g.183204798_183204801del , CM000663.1:g.183204798_183204801del GRCh37
NC_000001.9:g.181471421_181471424del NCBI36
NG_007079.2:g.54400_54403del

Transcript Alleles

HGVS Amino-acid change
ENST00000264144.5:c.2389_2392del MANE Select ENSP00000264144.4:p.Leu797MetfsTer?
ENST00000264144.4:c.2389_2392del ENSP00000264144.4:p.Leu797MetfsTer?
ENST00000493293.5:c.2389_2392del ENSP00000432063.1:p.Leu797MetfsTer?
NM_005562.2:c.2389_2392del NP_005553.2:p.Leu797MetfsTer?
NM_018891.2:c.2389_2392del NP_061486.2:p.Leu797MetfsTer?
XM_017001273.2:c.*80_*83del XP_016856762.1:n.*80_*83del
NM_005562.3:c.2389_2392del MANE Select NP_005553.2:p.Leu797MetfsTer?
NM_018891.3:c.2389_2392del NP_061486.2:p.Leu797MetfsTer?