Canonical Allele Identifier: CA2746913031
Gene: LAMC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183207860_183207861insATTTTT , CM000663.2:g.183207860_183207861insATTTTT GRCh38
NC_000001.10:g.183176995_183176996insATTTTT , CM000663.1:g.183176995_183176996insATTTTT GRCh37
NC_000001.9:g.181443618_181443619insATTTTT NCBI36
NG_007079.2:g.26597_26598insATTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000264144.5:c.80-21_80-20insATTTTT MANE Select ENSP00000264144.4:n.80-21_80-20insATTTTT
ENST00000264144.4:c.80-21_80-20insATTTTT ENSP00000264144.4:n.80-21_80-20insATTTTT
ENST00000493293.5:c.80-21_80-20insATTTTT ENSP00000432063.1:n.80-21_80-20insATTTTT
NM_005562.2:c.80-21_80-20insATTTTT NP_005553.2:n.80-21_80-20insATTTTT
NM_018891.2:c.80-21_80-20insATTTTT NP_061486.2:n.80-21_80-20insATTTTT
XM_017001273.2:c.80-21_80-20insATTTTT XP_016856762.1:n.80-21_80-20insATTTTT
NM_005562.3:c.80-21_80-20insATTTTT MANE Select NP_005553.2:n.80-21_80-20insATTTTT
NM_018891.3:c.80-21_80-20insATTTTT NP_061486.2:n.80-21_80-20insATTTTT