Canonical Allele Identifier: CA2641295906

Gene: LAMA3

Linked Data

• gnomAD v4: 18-23903137-AGTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23903141_23903143del , CM000680.2:g.23903141_23903143del	GRCh38
NC_000018.9:g.21483105_21483107del , CM000680.1:g.21483105_21483107del	GRCh37
NC_000018.8:g.19737103_19737105del	NCBI36
NG_007853.2:g.218544_218546del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1491+16_1491+18del MANE Plus Clinical	ENSP00000269217.5:n.1491+16_1491+18del
ENST00000313654.14:c.6318+16_6318+18del MANE Select	ENSP00000324532.8:n.6318+16_6318+18del
ENST00000649721.1:c.3210+16_3210+18del	ENSP00000497885.1:n.3210+16_3210+18del
ENST00000269217.10:c.1491+16_1491+18del	ENSP00000269217.5:n.1491+16_1491+18del
ENST00000313654.13:c.6318+16_6318+18del	ENSP00000324532.8:n.6318+16_6318+18del
ENST00000399516.7:c.6150+16_6150+18del	ENSP00000382432.2:n.6150+16_6150+18del
ENST00000586751.5:c.1096+16_1096+18del
ENST00000587184.5:c.1323+16_1323+18del	ENSP00000466557.1:n.1323+16_1323+18del
ENST00000588770.5:n.896+16_896+18del
NM_000227.4:c.1491+16_1491+18del	NP_000218.3:n.1491+16_1491+18del
NM_001127717.2:c.6150+16_6150+18del	NP_001121189.2:n.6150+16_6150+18del
NM_001127718.2:c.1323+16_1323+18del	NP_001121190.2:n.1323+16_1323+18del
NM_198129.2:c.6318+16_6318+18del	NP_937762.2:n.6318+16_6318+18del
XM_011525978.1:c.6345+16_6345+18del	XP_011524280.1:n.6345+16_6345+18del
XM_011525979.1:c.6336+16_6336+18del	XP_011524281.1:n.6336+16_6336+18del
XM_011525980.1:c.6327+16_6327+18del	XP_011524282.1:n.6327+16_6327+18del
XM_011525981.1:c.6213+16_6213+18del	XP_011524283.1:n.6213+16_6213+18del
XM_011525982.1:c.6345+16_6345+18del	XP_011524284.1:n.6345+16_6345+18del
XM_011525978.2:c.6345+16_6345+18del	XP_011524280.1:n.6345+16_6345+18del
XM_011525979.2:c.6336+16_6336+18del	XP_011524281.1:n.6336+16_6336+18del
XM_011525980.2:c.6327+16_6327+18del	XP_011524282.1:n.6327+16_6327+18del
XM_011525981.2:c.6213+16_6213+18del	XP_011524283.1:n.6213+16_6213+18del
XM_011525982.2:c.6345+16_6345+18del	XP_011524284.1:n.6345+16_6345+18del
XM_017025743.1:c.4197+16_4197+18del	XP_016881232.1:n.4197+16_4197+18del
XM_017025744.1:c.1887+16_1887+18del	XP_016881233.1:n.1887+16_1887+18del
XR_001753199.1:n.6586+16_6586+18del
NM_000227.5:c.1491+16_1491+18del	NP_000218.3:n.1491+16_1491+18del
NM_001127717.3:c.6150+16_6150+18del	NP_001121189.2:n.6150+16_6150+18del
NM_001127718.3:c.1323+16_1323+18del	NP_001121190.2:n.1323+16_1323+18del
NM_198129.3:c.6318+16_6318+18del	NP_937762.2:n.6318+16_6318+18del
NM_000227.6:c.1491+16_1491+18del MANE Plus Clinical	NP_000218.3:n.1491+16_1491+18del
NM_001127717.4:c.6150+16_6150+18del	NP_001121189.2:n.6150+16_6150+18del
NM_001127718.4:c.1323+16_1323+18del	NP_001121190.2:n.1323+16_1323+18del
NM_198129.4:c.6318+16_6318+18del MANE Select	NP_937762.2:n.6318+16_6318+18del