Canonical Allele Identifier: CA527259814
Gene: LAMC2 HGNC NCBI

Linked Data

gnomAD v2: 1-183176988-C-CTTTT
MyVariant Identifiers: chr1:g.183176988_183176989insTTTT (hg19) chr1:g.183207853_183207854insTTTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183207853_183207854insTTTT , CM000663.2:g.183207853_183207854insTTTT GRCh38
NC_000001.10:g.183176988_183176989insTTTT , CM000663.1:g.183176988_183176989insTTTT GRCh37
NC_000001.9:g.181443611_181443612insTTTT NCBI36
NG_007079.2:g.26590_26591insTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000264144.5:c.80-28_80-27insTTTT MANE Select ENSP00000264144.4:n.80-28_80-27insTTTT
ENST00000264144.4:c.80-28_80-27insTTTT ENSP00000264144.4:n.80-28_80-27insTTTT
ENST00000493293.5:c.80-28_80-27insTTTT ENSP00000432063.1:n.80-28_80-27insTTTT
NM_005562.2:c.80-28_80-27insTTTT NP_005553.2:n.80-28_80-27insTTTT
NM_018891.2:c.80-28_80-27insTTTT NP_061486.2:n.80-28_80-27insTTTT
XM_017001273.2:c.80-28_80-27insTTTT XP_016856762.1:n.80-28_80-27insTTTT
NM_005562.3:c.80-28_80-27insTTTT MANE Select NP_005553.2:n.80-28_80-27insTTTT
NM_018891.3:c.80-28_80-27insTTTT NP_061486.2:n.80-28_80-27insTTTT
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