Canonical Allele Identifier: CA527259881

Gene: LAMC2

Linked Data

• gnomAD v2: 1-183177004-C-CTTTTT
• gnomAD v3: 1-183207869-C-CTTTTT
• gnomAD v4: 1-183207869-C-CTTTTT
• MyVariant Identifiers: chr1:g.183177004_183177005insTTTTT (hg19) ; chr1:g.183207869_183207870insTTTTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183207871_183207872insTTTTT , CM000663.2:g.183207871_183207872insTTTTT	GRCh38
NC_000001.10:g.183177006_183177007insTTTTT , CM000663.1:g.183177006_183177007insTTTTT	GRCh37
NC_000001.9:g.181443629_181443630insTTTTT	NCBI36
NG_007079.2:g.26608_26609insTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264144.5:c.80-10_80-9insTTTTT MANE Select	ENSP00000264144.4:n.80-10_80-9insTTTTT
ENST00000264144.4:c.80-10_80-9insTTTTT	ENSP00000264144.4:n.80-10_80-9insTTTTT
ENST00000493293.5:c.80-10_80-9insTTTTT	ENSP00000432063.1:n.80-10_80-9insTTTTT
NM_005562.2:c.80-10_80-9insTTTTT	NP_005553.2:n.80-10_80-9insTTTTT
NM_018891.2:c.80-10_80-9insTTTTT	NP_061486.2:n.80-10_80-9insTTTTT
XM_017001273.2:c.80-10_80-9insTTTTT	XP_016856762.1:n.80-10_80-9insTTTTT
NM_005562.3:c.80-10_80-9insTTTTT MANE Select	NP_005553.2:n.80-10_80-9insTTTTT
NM_018891.3:c.80-10_80-9insTTTTT	NP_061486.2:n.80-10_80-9insTTTTT