Canonical Allele Identifier: CA2290324133

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23903369_23903370delinsCA , CM000680.2:g.23903369_23903370delinsCA	GRCh38
NC_000018.9:g.21483333_21483334delinsCA , CM000680.1:g.21483333_21483334delinsCA	GRCh37
NC_000018.8:g.19737331_19737332delinsCA	NCBI36
NG_007853.2:g.218772_218773delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1491+244_1491+245delinsCA MANE Plus Clinical	ENSP00000269217.5:n.1491+244_1491+245delinsCA
ENST00000313654.14:c.6318+244_6318+245delinsCA MANE Select	ENSP00000324532.8:n.6318+244_6318+245delinsCA
ENST00000649721.1:c.3210+244_3210+245delinsCA	ENSP00000497885.1:n.3210+244_3210+245delinsCA
ENST00000269217.10:c.1491+244_1491+245delinsCA	ENSP00000269217.5:n.1491+244_1491+245delinsCA
ENST00000313654.13:c.6318+244_6318+245delinsCA	ENSP00000324532.8:n.6318+244_6318+245delinsCA
ENST00000399516.7:c.6150+244_6150+245delinsCA	ENSP00000382432.2:n.6150+244_6150+245delinsCA
ENST00000586751.5:c.1096+244_1096+245delinsCA
ENST00000587184.5:c.1323+244_1323+245delinsCA	ENSP00000466557.1:n.1323+244_1323+245delinsCA
ENST00000588770.5:n.896+244_896+245delinsCA
NM_000227.4:c.1491+244_1491+245delinsCA	NP_000218.3:n.1491+244_1491+245delinsCA
NM_001127717.2:c.6150+244_6150+245delinsCA	NP_001121189.2:n.6150+244_6150+245delinsCA
NM_001127718.2:c.1323+244_1323+245delinsCA	NP_001121190.2:n.1323+244_1323+245delinsCA
NM_198129.2:c.6318+244_6318+245delinsCA	NP_937762.2:n.6318+244_6318+245delinsCA
XM_011525978.1:c.6345+244_6345+245delinsCA	XP_011524280.1:n.6345+244_6345+245delinsCA
XM_011525979.1:c.6336+244_6336+245delinsCA	XP_011524281.1:n.6336+244_6336+245delinsCA
XM_011525980.1:c.6327+244_6327+245delinsCA	XP_011524282.1:n.6327+244_6327+245delinsCA
XM_011525981.1:c.6213+244_6213+245delinsCA	XP_011524283.1:n.6213+244_6213+245delinsCA
XM_011525982.1:c.6345+244_6345+245delinsCA	XP_011524284.1:n.6345+244_6345+245delinsCA
XM_011525978.2:c.6345+244_6345+245delinsCA	XP_011524280.1:n.6345+244_6345+245delinsCA
XM_011525979.2:c.6336+244_6336+245delinsCA	XP_011524281.1:n.6336+244_6336+245delinsCA
XM_011525980.2:c.6327+244_6327+245delinsCA	XP_011524282.1:n.6327+244_6327+245delinsCA
XM_011525981.2:c.6213+244_6213+245delinsCA	XP_011524283.1:n.6213+244_6213+245delinsCA
XM_011525982.2:c.6345+244_6345+245delinsCA	XP_011524284.1:n.6345+244_6345+245delinsCA
XM_017025743.1:c.4197+244_4197+245delinsCA	XP_016881232.1:n.4197+244_4197+245delinsCA
XM_017025744.1:c.1887+244_1887+245delinsCA	XP_016881233.1:n.1887+244_1887+245delinsCA
XR_001753199.1:n.6586+244_6586+245delinsCA
NM_000227.5:c.1491+244_1491+245delinsCA	NP_000218.3:n.1491+244_1491+245delinsCA
NM_001127717.3:c.6150+244_6150+245delinsCA	NP_001121189.2:n.6150+244_6150+245delinsCA
NM_001127718.3:c.1323+244_1323+245delinsCA	NP_001121190.2:n.1323+244_1323+245delinsCA
NM_198129.3:c.6318+244_6318+245delinsCA	NP_937762.2:n.6318+244_6318+245delinsCA
NM_000227.6:c.1491+244_1491+245delinsCA MANE Plus Clinical	NP_000218.3:n.1491+244_1491+245delinsCA
NM_001127717.4:c.6150+244_6150+245delinsCA	NP_001121189.2:n.6150+244_6150+245delinsCA
NM_001127718.4:c.1323+244_1323+245delinsCA	NP_001121190.2:n.1323+244_1323+245delinsCA
NM_198129.4:c.6318+244_6318+245delinsCA MANE Select	NP_937762.2:n.6318+244_6318+245delinsCA