Canonical Allele Identifier: CA2649463379

Gene: LAMC2

Linked Data

• gnomAD v4: 1-183207864-G-GTTTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183207865_183207866insTTTTTTTTTT , CM000663.2:g.183207865_183207866insTTTTTTTTTT	GRCh38
NC_000001.10:g.183177000_183177001insTTTTTTTTTT , CM000663.1:g.183177000_183177001insTTTTTTTTTT	GRCh37
NC_000001.9:g.181443623_181443624insTTTTTTTTTT	NCBI36
NG_007079.2:g.26602_26603insTTTTTTTTTT

Transcript Alleles

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