Canonical Allele Identifier: CA2290324152

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23903443_23903444delinsTC , CM000680.2:g.23903443_23903444delinsTC	GRCh38
NC_000018.9:g.21483407_21483408delinsTC , CM000680.1:g.21483407_21483408delinsTC	GRCh37
NC_000018.8:g.19737405_19737406delinsTC	NCBI36
NG_007853.2:g.218846_218847delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1491+318_1491+319delinsTC MANE Plus Clinical	ENSP00000269217.5:n.1491+318_1491+319delinsTC
ENST00000313654.14:c.6318+318_6318+319delinsTC MANE Select	ENSP00000324532.8:n.6318+318_6318+319delinsTC
ENST00000649721.1:c.3210+318_3210+319delinsTC	ENSP00000497885.1:n.3210+318_3210+319delinsTC
ENST00000269217.10:c.1491+318_1491+319delinsTC	ENSP00000269217.5:n.1491+318_1491+319delinsTC
ENST00000313654.13:c.6318+318_6318+319delinsTC	ENSP00000324532.8:n.6318+318_6318+319delinsTC
ENST00000399516.7:c.6150+318_6150+319delinsTC	ENSP00000382432.2:n.6150+318_6150+319delinsTC
ENST00000586751.5:c.1096+318_1096+319delinsTC
ENST00000587184.5:c.1323+318_1323+319delinsTC	ENSP00000466557.1:n.1323+318_1323+319delinsTC
ENST00000588770.5:n.896+318_896+319delinsTC
NM_000227.4:c.1491+318_1491+319delinsTC	NP_000218.3:n.1491+318_1491+319delinsTC
NM_001127717.2:c.6150+318_6150+319delinsTC	NP_001121189.2:n.6150+318_6150+319delinsTC
NM_001127718.2:c.1323+318_1323+319delinsTC	NP_001121190.2:n.1323+318_1323+319delinsTC
NM_198129.2:c.6318+318_6318+319delinsTC	NP_937762.2:n.6318+318_6318+319delinsTC
XM_011525978.1:c.6345+318_6345+319delinsTC	XP_011524280.1:n.6345+318_6345+319delinsTC
XM_011525979.1:c.6336+318_6336+319delinsTC	XP_011524281.1:n.6336+318_6336+319delinsTC
XM_011525980.1:c.6327+318_6327+319delinsTC	XP_011524282.1:n.6327+318_6327+319delinsTC
XM_011525981.1:c.6213+318_6213+319delinsTC	XP_011524283.1:n.6213+318_6213+319delinsTC
XM_011525982.1:c.6345+318_6345+319delinsTC	XP_011524284.1:n.6345+318_6345+319delinsTC
XM_011525978.2:c.6345+318_6345+319delinsTC	XP_011524280.1:n.6345+318_6345+319delinsTC
XM_011525979.2:c.6336+318_6336+319delinsTC	XP_011524281.1:n.6336+318_6336+319delinsTC
XM_011525980.2:c.6327+318_6327+319delinsTC	XP_011524282.1:n.6327+318_6327+319delinsTC
XM_011525981.2:c.6213+318_6213+319delinsTC	XP_011524283.1:n.6213+318_6213+319delinsTC
XM_011525982.2:c.6345+318_6345+319delinsTC	XP_011524284.1:n.6345+318_6345+319delinsTC
XM_017025743.1:c.4197+318_4197+319delinsTC	XP_016881232.1:n.4197+318_4197+319delinsTC
XM_017025744.1:c.1887+318_1887+319delinsTC	XP_016881233.1:n.1887+318_1887+319delinsTC
XR_001753199.1:n.6586+318_6586+319delinsTC
NM_000227.5:c.1491+318_1491+319delinsTC	NP_000218.3:n.1491+318_1491+319delinsTC
NM_001127717.3:c.6150+318_6150+319delinsTC	NP_001121189.2:n.6150+318_6150+319delinsTC
NM_001127718.3:c.1323+318_1323+319delinsTC	NP_001121190.2:n.1323+318_1323+319delinsTC
NM_198129.3:c.6318+318_6318+319delinsTC	NP_937762.2:n.6318+318_6318+319delinsTC
NM_000227.6:c.1491+318_1491+319delinsTC MANE Plus Clinical	NP_000218.3:n.1491+318_1491+319delinsTC
NM_001127717.4:c.6150+318_6150+319delinsTC	NP_001121189.2:n.6150+318_6150+319delinsTC
NM_001127718.4:c.1323+318_1323+319delinsTC	NP_001121190.2:n.1323+318_1323+319delinsTC
NM_198129.4:c.6318+318_6318+319delinsTC MANE Select	NP_937762.2:n.6318+318_6318+319delinsTC