Canonical Allele Identifier: CA527259809

Gene: LAMC2

Linked Data

• gnomAD v2: 1-183176987-A-ATTT
• gnomAD v3: 1-183207852-A-ATTT
• gnomAD v4: 1-183207852-A-ATTT
• MyVariant Identifiers: chr1:g.183176987_183176988insTTT (hg19) ; chr1:g.183207852_183207853insTTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183207852_183207853insTTT , CM000663.2:g.183207852_183207853insTTT	GRCh38
NC_000001.10:g.183176987_183176988insTTT , CM000663.1:g.183176987_183176988insTTT	GRCh37
NC_000001.9:g.181443610_181443611insTTT	NCBI36
NG_007079.2:g.26589_26590insTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264144.5:c.80-29_80-28insTTT MANE Select	ENSP00000264144.4:n.80-29_80-28insTTT
ENST00000264144.4:c.80-29_80-28insTTT	ENSP00000264144.4:n.80-29_80-28insTTT
ENST00000493293.5:c.80-29_80-28insTTT	ENSP00000432063.1:n.80-29_80-28insTTT
NM_005562.2:c.80-29_80-28insTTT	NP_005553.2:n.80-29_80-28insTTT
NM_018891.2:c.80-29_80-28insTTT	NP_061486.2:n.80-29_80-28insTTT
XM_017001273.2:c.80-29_80-28insTTT	XP_016856762.1:n.80-29_80-28insTTT
NM_005562.3:c.80-29_80-28insTTT MANE Select	NP_005553.2:n.80-29_80-28insTTT
NM_018891.3:c.80-29_80-28insTTT	NP_061486.2:n.80-29_80-28insTTT