Canonical Allele Identifier: CA2649463351

Gene: LAMC2

Linked Data

• gnomAD v4: 1-183207835-GTTTTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183207846_183207850del , CM000663.2:g.183207846_183207850del	GRCh38
NC_000001.10:g.183176981_183176985del , CM000663.1:g.183176981_183176985del	GRCh37
NC_000001.9:g.181443604_181443608del	NCBI36
NG_007079.2:g.26583_26587del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264144.5:c.80-35_80-31del MANE Select	ENSP00000264144.4:n.80-35_80-31del
ENST00000264144.4:c.80-35_80-31del	ENSP00000264144.4:n.80-35_80-31del
ENST00000493293.5:c.80-35_80-31del	ENSP00000432063.1:n.80-35_80-31del
NM_005562.2:c.80-35_80-31del	NP_005553.2:n.80-35_80-31del
NM_018891.2:c.80-35_80-31del	NP_061486.2:n.80-35_80-31del
XM_017001273.2:c.80-35_80-31del	XP_016856762.1:n.80-35_80-31del
NM_005562.3:c.80-35_80-31del MANE Select	NP_005553.2:n.80-35_80-31del
NM_018891.3:c.80-35_80-31del	NP_061486.2:n.80-35_80-31del