Canonical Allele Identifier: CA1009927399
Gene: LAMC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183207865_183207866insTTT , CM000663.2:g.183207865_183207866insTTT GRCh38
NC_000001.10:g.183177000_183177001insTTT , CM000663.1:g.183177000_183177001insTTT GRCh37
NC_000001.9:g.181443623_181443624insTTT NCBI36
NG_007079.2:g.26602_26603insTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000264144.5:c.80-16_80-15insTTT MANE Select ENSP00000264144.4:n.80-16_80-15insTTT
ENST00000264144.4:c.80-16_80-15insTTT ENSP00000264144.4:n.80-16_80-15insTTT
ENST00000493293.5:c.80-16_80-15insTTT ENSP00000432063.1:n.80-16_80-15insTTT
NM_005562.2:c.80-16_80-15insTTT NP_005553.2:n.80-16_80-15insTTT
NM_018891.2:c.80-16_80-15insTTT NP_061486.2:n.80-16_80-15insTTT
XM_017001273.2:c.80-16_80-15insTTT XP_016856762.1:n.80-16_80-15insTTT
NM_005562.3:c.80-16_80-15insTTT MANE Select NP_005553.2:n.80-16_80-15insTTT
NM_018891.3:c.80-16_80-15insTTT NP_061486.2:n.80-16_80-15insTTT