Canonical Allele Identifier: CA2641295986

Gene: LAMA3

Linked Data

• gnomAD v4: 18-23903244-A-ATT

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23903244_23903245insTT , CM000680.2:g.23903244_23903245insTT	GRCh38
NC_000018.9:g.21483208_21483209insTT , CM000680.1:g.21483208_21483209insTT	GRCh37
NC_000018.8:g.19737206_19737207insTT	NCBI36
NG_007853.2:g.218647_218648insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1491+119_1491+120insTT MANE Plus Clinical	ENSP00000269217.5:n.1491+119_1491+120insTT
ENST00000313654.14:c.6318+119_6318+120insTT MANE Select	ENSP00000324532.8:n.6318+119_6318+120insTT
ENST00000649721.1:c.3210+119_3210+120insTT	ENSP00000497885.1:n.3210+119_3210+120insTT
ENST00000269217.10:c.1491+119_1491+120insTT	ENSP00000269217.5:n.1491+119_1491+120insTT
ENST00000313654.13:c.6318+119_6318+120insTT	ENSP00000324532.8:n.6318+119_6318+120insTT
ENST00000399516.7:c.6150+119_6150+120insTT	ENSP00000382432.2:n.6150+119_6150+120insTT
ENST00000586751.5:c.1096+119_1096+120insTT
ENST00000587184.5:c.1323+119_1323+120insTT	ENSP00000466557.1:n.1323+119_1323+120insTT
ENST00000588770.5:n.896+119_896+120insTT
NM_000227.4:c.1491+119_1491+120insTT	NP_000218.3:n.1491+119_1491+120insTT
NM_001127717.2:c.6150+119_6150+120insTT	NP_001121189.2:n.6150+119_6150+120insTT
NM_001127718.2:c.1323+119_1323+120insTT	NP_001121190.2:n.1323+119_1323+120insTT
NM_198129.2:c.6318+119_6318+120insTT	NP_937762.2:n.6318+119_6318+120insTT
XM_011525978.1:c.6345+119_6345+120insTT	XP_011524280.1:n.6345+119_6345+120insTT
XM_011525979.1:c.6336+119_6336+120insTT	XP_011524281.1:n.6336+119_6336+120insTT
XM_011525980.1:c.6327+119_6327+120insTT	XP_011524282.1:n.6327+119_6327+120insTT
XM_011525981.1:c.6213+119_6213+120insTT	XP_011524283.1:n.6213+119_6213+120insTT
XM_011525982.1:c.6345+119_6345+120insTT	XP_011524284.1:n.6345+119_6345+120insTT
XM_011525978.2:c.6345+119_6345+120insTT	XP_011524280.1:n.6345+119_6345+120insTT
XM_011525979.2:c.6336+119_6336+120insTT	XP_011524281.1:n.6336+119_6336+120insTT
XM_011525980.2:c.6327+119_6327+120insTT	XP_011524282.1:n.6327+119_6327+120insTT
XM_011525981.2:c.6213+119_6213+120insTT	XP_011524283.1:n.6213+119_6213+120insTT
XM_011525982.2:c.6345+119_6345+120insTT	XP_011524284.1:n.6345+119_6345+120insTT
XM_017025743.1:c.4197+119_4197+120insTT	XP_016881232.1:n.4197+119_4197+120insTT
XM_017025744.1:c.1887+119_1887+120insTT	XP_016881233.1:n.1887+119_1887+120insTT
XR_001753199.1:n.6586+119_6586+120insTT
NM_000227.5:c.1491+119_1491+120insTT	NP_000218.3:n.1491+119_1491+120insTT
NM_001127717.3:c.6150+119_6150+120insTT	NP_001121189.2:n.6150+119_6150+120insTT
NM_001127718.3:c.1323+119_1323+120insTT	NP_001121190.2:n.1323+119_1323+120insTT
NM_198129.3:c.6318+119_6318+120insTT	NP_937762.2:n.6318+119_6318+120insTT
NM_000227.6:c.1491+119_1491+120insTT MANE Plus Clinical	NP_000218.3:n.1491+119_1491+120insTT
NM_001127717.4:c.6150+119_6150+120insTT	NP_001121189.2:n.6150+119_6150+120insTT
NM_001127718.4:c.1323+119_1323+120insTT	NP_001121190.2:n.1323+119_1323+120insTT
NM_198129.4:c.6318+119_6318+120insTT MANE Select	NP_937762.2:n.6318+119_6318+120insTT