Canonical Allele Identifier: CA2649463369

Gene: LAMC2

Linked Data

• gnomAD v4: 1-183207850-T-TTTTC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.183207850_183207851insTTTC , CM000663.2:g.183207850_183207851insTTTC	GRCh38
NC_000001.10:g.183176985_183176986insTTTC , CM000663.1:g.183176985_183176986insTTTC	GRCh37
NC_000001.9:g.181443608_181443609insTTTC	NCBI36
NG_007079.2:g.26587_26588insTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264144.5:c.80-31_80-30insTTTC MANE Select	ENSP00000264144.4:n.80-31_80-30insTTTC
ENST00000264144.4:c.80-31_80-30insTTTC	ENSP00000264144.4:n.80-31_80-30insTTTC
ENST00000493293.5:c.80-31_80-30insTTTC	ENSP00000432063.1:n.80-31_80-30insTTTC
NM_005562.2:c.80-31_80-30insTTTC	NP_005553.2:n.80-31_80-30insTTTC
NM_018891.2:c.80-31_80-30insTTTC	NP_061486.2:n.80-31_80-30insTTTC
XM_017001273.2:c.80-31_80-30insTTTC	XP_016856762.1:n.80-31_80-30insTTTC
NM_005562.3:c.80-31_80-30insTTTC MANE Select	NP_005553.2:n.80-31_80-30insTTTC
NM_018891.3:c.80-31_80-30insTTTC	NP_061486.2:n.80-31_80-30insTTTC