Canonical Allele Identifier: CA1282209

Gene: LAMC2

Linked Data

• dbSNP Id: rs1553264610
• ExAC: 1:183176973 T / TTG
• gnomAD v2: 1-183176973-T-TTG
• gnomAD v3: 1-183207838-T-TTG
• gnomAD v4: 1-183207838-T-TTG
• MyVariant Identifiers: chr1:g.183176973_183176974insTG (hg19) ; chr1:g.183207838_183207839insTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183207839_183207840insGT , CM000663.2:g.183207839_183207840insGT	GRCh38
NC_000001.10:g.183176974_183176975insGT , CM000663.1:g.183176974_183176975insGT	GRCh37
NC_000001.9:g.181443597_181443598insGT	NCBI36
NG_007079.2:g.26576_26577insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264144.5:c.80-42_80-41insGT MANE Select	ENSP00000264144.4:n.80-42_80-41insGT
ENST00000264144.4:c.80-42_80-41insGT	ENSP00000264144.4:n.80-42_80-41insGT
ENST00000493293.5:c.80-42_80-41insGT	ENSP00000432063.1:n.80-42_80-41insGT
NM_005562.2:c.80-42_80-41insGT	NP_005553.2:n.80-42_80-41insGT
NM_018891.2:c.80-42_80-41insGT	NP_061486.2:n.80-42_80-41insGT
XM_017001273.2:c.80-42_80-41insGT	XP_016856762.1:n.80-42_80-41insGT
NM_005562.3:c.80-42_80-41insGT MANE Select	NP_005553.2:n.80-42_80-41insGT
NM_018891.3:c.80-42_80-41insGT	NP_061486.2:n.80-42_80-41insGT