Canonical Allele Identifier: CA2641293571

Gene: LAMA3

Linked Data

• gnomAD v4: 18-23873060-AGGCGGTCAGCCTGCAGCATGGGAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23873064_23873087del , CM000680.2:g.23873064_23873087del	GRCh38
NC_000018.9:g.21453028_21453051del , CM000680.1:g.21453028_21453051del	GRCh37
NC_000018.8:g.19707026_19707049del	NCBI36
NG_007853.2:g.188467_188490del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.20_43del MANE Plus Clinical	ENSP00000269217.5:p.Arg7_Trp14del
ENST00000313654.14:c.4998+1403_4998+1426del MANE Select	ENSP00000324532.8:n.4998+1403_4998+1426del
ENST00000649721.1:c.1890+1403_1890+1426del	ENSP00000497885.1:n.1890+1403_1890+1426del
ENST00000269217.10:c.20_43del	ENSP00000269217.5:p.Arg7_Trp14del
ENST00000313654.13:c.4998+1403_4998+1426del	ENSP00000324532.8:n.4998+1403_4998+1426del
ENST00000399516.7:c.4998+1403_4998+1426del	ENSP00000382432.2:n.4998+1403_4998+1426del
ENST00000587184.5:c.20_43del	ENSP00000466557.1:p.Arg7_Trp14del
NM_000227.4:c.20_43del	NP_000218.3:p.Arg7_Trp14del
NM_001127717.2:c.4998+1403_4998+1426del	NP_001121189.2:n.4998+1403_4998+1426del
NM_001127718.2:c.20_43del	NP_001121190.2:p.Arg7_Trp14del
NM_198129.2:c.4998+1403_4998+1426del	NP_937762.2:n.4998+1403_4998+1426del
XM_011525978.1:c.5025+1403_5025+1426del	XP_011524280.1:n.5025+1403_5025+1426del
XM_011525979.1:c.5016+1403_5016+1426del	XP_011524281.1:n.5016+1403_5016+1426del
XM_011525980.1:c.5007+1403_5007+1426del	XP_011524282.1:n.5007+1403_5007+1426del
XM_011525981.1:c.4893+1403_4893+1426del	XP_011524283.1:n.4893+1403_4893+1426del
XM_011525982.1:c.5025+1403_5025+1426del	XP_011524284.1:n.5025+1403_5025+1426del
XM_011525978.2:c.5025+1403_5025+1426del	XP_011524280.1:n.5025+1403_5025+1426del
XM_011525979.2:c.5016+1403_5016+1426del	XP_011524281.1:n.5016+1403_5016+1426del
XM_011525980.2:c.5007+1403_5007+1426del	XP_011524282.1:n.5007+1403_5007+1426del
XM_011525981.2:c.4893+1403_4893+1426del	XP_011524283.1:n.4893+1403_4893+1426del
XM_011525982.2:c.5025+1403_5025+1426del	XP_011524284.1:n.5025+1403_5025+1426del
XM_017025743.1:c.2877+1403_2877+1426del	XP_016881232.1:n.2877+1403_2877+1426del
XM_017025744.1:c.567+1403_567+1426del	XP_016881233.1:n.567+1403_567+1426del
XR_001753199.1:n.5266+1403_5266+1426del
NM_000227.5:c.20_43del	NP_000218.3:p.Arg7_Trp14del
NM_001127717.3:c.4998+1403_4998+1426del	NP_001121189.2:n.4998+1403_4998+1426del
NM_001127718.3:c.20_43del	NP_001121190.2:p.Arg7_Trp14del
NM_198129.3:c.4998+1403_4998+1426del	NP_937762.2:n.4998+1403_4998+1426del
NM_000227.6:c.20_43del MANE Plus Clinical	NP_000218.3:p.Arg7_Trp14del
NM_001127717.4:c.4998+1403_4998+1426del	NP_001121189.2:n.4998+1403_4998+1426del
NM_001127718.4:c.20_43del	NP_001121190.2:p.Arg7_Trp14del
NM_198129.4:c.4998+1403_4998+1426del MANE Select	NP_937762.2:n.4998+1403_4998+1426del