Canonical Allele Identifier: CA2847562906

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23903157_23903158insTTTTACTTTC , CM000680.2:g.23903157_23903158insTTTTACTTTC	GRCh38
NC_000018.9:g.21483121_21483122insTTTTACTTTC , CM000680.1:g.21483121_21483122insTTTTACTTTC	GRCh37
NC_000018.8:g.19737119_19737120insTTTTACTTTC	NCBI36
NG_007853.2:g.218560_218561insTTTTACTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1491+32_1491+33insTTTTACTTTC MANE Plus Clinical	ENSP00000269217.5:n.1491+32_1491+33insTTTTACTTTC
ENST00000313654.14:c.6318+32_6318+33insTTTTACTTTC MANE Select	ENSP00000324532.8:n.6318+32_6318+33insTTTTACTTTC
ENST00000649721.1:c.3210+32_3210+33insTTTTACTTTC	ENSP00000497885.1:n.3210+32_3210+33insTTTTACTTTC
ENST00000269217.10:c.1491+32_1491+33insTTTTACTTTC	ENSP00000269217.5:n.1491+32_1491+33insTTTTACTTTC
ENST00000313654.13:c.6318+32_6318+33insTTTTACTTTC	ENSP00000324532.8:n.6318+32_6318+33insTTTTACTTTC
ENST00000399516.7:c.6150+32_6150+33insTTTTACTTTC	ENSP00000382432.2:n.6150+32_6150+33insTTTTACTTTC
ENST00000586751.5:c.1096+32_1096+33insTTTTACTTTC
ENST00000587184.5:c.1323+32_1323+33insTTTTACTTTC	ENSP00000466557.1:n.1323+32_1323+33insTTTTACTTTC
ENST00000588770.5:n.896+32_896+33insTTTTACTTTC
NM_000227.4:c.1491+32_1491+33insTTTTACTTTC	NP_000218.3:n.1491+32_1491+33insTTTTACTTTC
NM_001127717.2:c.6150+32_6150+33insTTTTACTTTC	NP_001121189.2:n.6150+32_6150+33insTTTTACTTTC
NM_001127718.2:c.1323+32_1323+33insTTTTACTTTC	NP_001121190.2:n.1323+32_1323+33insTTTTACTTTC
NM_198129.2:c.6318+32_6318+33insTTTTACTTTC	NP_937762.2:n.6318+32_6318+33insTTTTACTTTC
XM_011525978.1:c.6345+32_6345+33insTTTTACTTTC	XP_011524280.1:n.6345+32_6345+33insTTTTACTTTC
XM_011525979.1:c.6336+32_6336+33insTTTTACTTTC	XP_011524281.1:n.6336+32_6336+33insTTTTACTTTC
XM_011525980.1:c.6327+32_6327+33insTTTTACTTTC	XP_011524282.1:n.6327+32_6327+33insTTTTACTTTC
XM_011525981.1:c.6213+32_6213+33insTTTTACTTTC	XP_011524283.1:n.6213+32_6213+33insTTTTACTTTC
XM_011525982.1:c.6345+32_6345+33insTTTTACTTTC	XP_011524284.1:n.6345+32_6345+33insTTTTACTTTC
XM_011525978.2:c.6345+32_6345+33insTTTTACTTTC	XP_011524280.1:n.6345+32_6345+33insTTTTACTTTC
XM_011525979.2:c.6336+32_6336+33insTTTTACTTTC	XP_011524281.1:n.6336+32_6336+33insTTTTACTTTC
XM_011525980.2:c.6327+32_6327+33insTTTTACTTTC	XP_011524282.1:n.6327+32_6327+33insTTTTACTTTC
XM_011525981.2:c.6213+32_6213+33insTTTTACTTTC	XP_011524283.1:n.6213+32_6213+33insTTTTACTTTC
XM_011525982.2:c.6345+32_6345+33insTTTTACTTTC	XP_011524284.1:n.6345+32_6345+33insTTTTACTTTC
XM_017025743.1:c.4197+32_4197+33insTTTTACTTTC	XP_016881232.1:n.4197+32_4197+33insTTTTACTTTC
XM_017025744.1:c.1887+32_1887+33insTTTTACTTTC	XP_016881233.1:n.1887+32_1887+33insTTTTACTTTC
XR_001753199.1:n.6586+32_6586+33insTTTTACTTTC
NM_000227.5:c.1491+32_1491+33insTTTTACTTTC	NP_000218.3:n.1491+32_1491+33insTTTTACTTTC
NM_001127717.3:c.6150+32_6150+33insTTTTACTTTC	NP_001121189.2:n.6150+32_6150+33insTTTTACTTTC
NM_001127718.3:c.1323+32_1323+33insTTTTACTTTC	NP_001121190.2:n.1323+32_1323+33insTTTTACTTTC
NM_198129.3:c.6318+32_6318+33insTTTTACTTTC	NP_937762.2:n.6318+32_6318+33insTTTTACTTTC
NM_000227.6:c.1491+32_1491+33insTTTTACTTTC MANE Plus Clinical	NP_000218.3:n.1491+32_1491+33insTTTTACTTTC
NM_001127717.4:c.6150+32_6150+33insTTTTACTTTC	NP_001121189.2:n.6150+32_6150+33insTTTTACTTTC
NM_001127718.4:c.1323+32_1323+33insTTTTACTTTC	NP_001121190.2:n.1323+32_1323+33insTTTTACTTTC
NM_198129.4:c.6318+32_6318+33insTTTTACTTTC MANE Select	NP_937762.2:n.6318+32_6318+33insTTTTACTTTC