Canonical Allele Identifier: CA527259830

Gene: LAMC2

Linked Data

• gnomAD v2: 1-183176990-A-ATTT
• gnomAD v3: 1-183207855-A-ATTT
• gnomAD v4: 1-183207855-A-ATTT
• MyVariant Identifiers: chr1:g.183176990_183176991insTTT (hg19) ; chr1:g.183207855_183207856insTTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183207856_183207857insTTT , CM000663.2:g.183207856_183207857insTTT	GRCh38
NC_000001.10:g.183176991_183176992insTTT , CM000663.1:g.183176991_183176992insTTT	GRCh37
NC_000001.9:g.181443614_181443615insTTT	NCBI36
NG_007079.2:g.26593_26594insTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264144.5:c.80-25_80-24insTTT MANE Select	ENSP00000264144.4:n.80-25_80-24insTTT
ENST00000264144.4:c.80-25_80-24insTTT	ENSP00000264144.4:n.80-25_80-24insTTT
ENST00000493293.5:c.80-25_80-24insTTT	ENSP00000432063.1:n.80-25_80-24insTTT
NM_005562.2:c.80-25_80-24insTTT	NP_005553.2:n.80-25_80-24insTTT
NM_018891.2:c.80-25_80-24insTTT	NP_061486.2:n.80-25_80-24insTTT
XM_017001273.2:c.80-25_80-24insTTT	XP_016856762.1:n.80-25_80-24insTTT
NM_005562.3:c.80-25_80-24insTTT MANE Select	NP_005553.2:n.80-25_80-24insTTT
NM_018891.3:c.80-25_80-24insTTT	NP_061486.2:n.80-25_80-24insTTT