Canonical Allele Identifier: CA2290324097
Gene: LAMA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23903286_23903287delinsAG , CM000680.2:g.23903286_23903287delinsAG GRCh38
NC_000018.9:g.21483250_21483251delinsAG , CM000680.1:g.21483250_21483251delinsAG GRCh37
NC_000018.8:g.19737248_19737249delinsAG NCBI36
NG_007853.2:g.218689_218690delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000269217.11:c.1491+161_1491+162delinsAG MANE Plus Clinical ENSP00000269217.5:n.1491+161_1491+162delinsAG
ENST00000313654.14:c.6318+161_6318+162delinsAG MANE Select ENSP00000324532.8:n.6318+161_6318+162delinsAG
ENST00000649721.1:c.3210+161_3210+162delinsAG ENSP00000497885.1:n.3210+161_3210+162delinsAG
ENST00000269217.10:c.1491+161_1491+162delinsAG ENSP00000269217.5:n.1491+161_1491+162delinsAG
ENST00000313654.13:c.6318+161_6318+162delinsAG ENSP00000324532.8:n.6318+161_6318+162delinsAG
ENST00000399516.7:c.6150+161_6150+162delinsAG ENSP00000382432.2:n.6150+161_6150+162delinsAG
ENST00000586751.5:c.1096+161_1096+162delinsAG
ENST00000587184.5:c.1323+161_1323+162delinsAG ENSP00000466557.1:n.1323+161_1323+162delinsAG
ENST00000588770.5:n.896+161_896+162delinsAG
NM_000227.4:c.1491+161_1491+162delinsAG NP_000218.3:n.1491+161_1491+162delinsAG
NM_001127717.2:c.6150+161_6150+162delinsAG NP_001121189.2:n.6150+161_6150+162delinsAG
NM_001127718.2:c.1323+161_1323+162delinsAG NP_001121190.2:n.1323+161_1323+162delinsAG
NM_198129.2:c.6318+161_6318+162delinsAG NP_937762.2:n.6318+161_6318+162delinsAG
XM_011525978.1:c.6345+161_6345+162delinsAG XP_011524280.1:n.6345+161_6345+162delinsAG
XM_011525979.1:c.6336+161_6336+162delinsAG XP_011524281.1:n.6336+161_6336+162delinsAG
XM_011525980.1:c.6327+161_6327+162delinsAG XP_011524282.1:n.6327+161_6327+162delinsAG
XM_011525981.1:c.6213+161_6213+162delinsAG XP_011524283.1:n.6213+161_6213+162delinsAG
XM_011525982.1:c.6345+161_6345+162delinsAG XP_011524284.1:n.6345+161_6345+162delinsAG
XM_011525978.2:c.6345+161_6345+162delinsAG XP_011524280.1:n.6345+161_6345+162delinsAG
XM_011525979.2:c.6336+161_6336+162delinsAG XP_011524281.1:n.6336+161_6336+162delinsAG
XM_011525980.2:c.6327+161_6327+162delinsAG XP_011524282.1:n.6327+161_6327+162delinsAG
XM_011525981.2:c.6213+161_6213+162delinsAG XP_011524283.1:n.6213+161_6213+162delinsAG
XM_011525982.2:c.6345+161_6345+162delinsAG XP_011524284.1:n.6345+161_6345+162delinsAG
XM_017025743.1:c.4197+161_4197+162delinsAG XP_016881232.1:n.4197+161_4197+162delinsAG
XM_017025744.1:c.1887+161_1887+162delinsAG XP_016881233.1:n.1887+161_1887+162delinsAG
XR_001753199.1:n.6586+161_6586+162delinsAG
NM_000227.5:c.1491+161_1491+162delinsAG NP_000218.3:n.1491+161_1491+162delinsAG
NM_001127717.3:c.6150+161_6150+162delinsAG NP_001121189.2:n.6150+161_6150+162delinsAG
NM_001127718.3:c.1323+161_1323+162delinsAG NP_001121190.2:n.1323+161_1323+162delinsAG
NM_198129.3:c.6318+161_6318+162delinsAG NP_937762.2:n.6318+161_6318+162delinsAG
NM_000227.6:c.1491+161_1491+162delinsAG MANE Plus Clinical NP_000218.3:n.1491+161_1491+162delinsAG
NM_001127717.4:c.6150+161_6150+162delinsAG NP_001121189.2:n.6150+161_6150+162delinsAG
NM_001127718.4:c.1323+161_1323+162delinsAG NP_001121190.2:n.1323+161_1323+162delinsAG
NM_198129.4:c.6318+161_6318+162delinsAG MANE Select NP_937762.2:n.6318+161_6318+162delinsAG