Canonical Allele Identifier: CA2641295904

Gene: LAMA3

Linked Data

• gnomAD v4: 18-23903135-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23903135_23903136insC , CM000680.2:g.23903135_23903136insC	GRCh38
NC_000018.9:g.21483099_21483100insC , CM000680.1:g.21483099_21483100insC	GRCh37
NC_000018.8:g.19737097_19737098insC	NCBI36
NG_007853.2:g.218538_218539insC

Transcript Alleles

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