Canonical Allele Identifier: CA1211821081
Gene: LAMC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183232112_183232113delinsTG , CM000663.2:g.183232112_183232113delinsTG GRCh38
NC_000001.10:g.183201247_183201248delinsTG , CM000663.1:g.183201247_183201248delinsTG GRCh37
NC_000001.9:g.181467870_181467871delinsTG NCBI36
NG_007079.2:g.50849_50850delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000264144.5:c.1858-75_1858-74delinsTG MANE Select ENSP00000264144.4:n.1858-75_1858-74delinsTG
ENST00000264144.4:c.1858-75_1858-74delinsTG ENSP00000264144.4:n.1858-75_1858-74delinsTG
ENST00000493293.5:c.1858-75_1858-74delinsTG ENSP00000432063.1:n.1858-75_1858-74delinsTG
NM_005562.2:c.1858-75_1858-74delinsTG NP_005553.2:n.1858-75_1858-74delinsTG
NM_018891.2:c.1858-75_1858-74delinsTG NP_061486.2:n.1858-75_1858-74delinsTG
XM_017001273.2:c.1858-75_1858-74delinsTG XP_016856762.1:n.1858-75_1858-74delinsTG
NM_005562.3:c.1858-75_1858-74delinsTG MANE Select NP_005553.2:n.1858-75_1858-74delinsTG
NM_018891.3:c.1858-75_1858-74delinsTG NP_061486.2:n.1858-75_1858-74delinsTG