Canonical Allele Identifier: CA402063352
Gene: LAMA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23928222G>C , CM000680.2:g.23928222G>C GRCh38
NC_000018.9:g.21508186G>C , CM000680.1:g.21508186G>C GRCh37
NC_000018.8:g.19762184G>C NCBI36
NG_007853.2:g.243625G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269217.11:c.3450G>C MANE Plus Clinical ENSP00000269217.5:p.Lys1150Asn
ENST00000313654.14:c.8277G>C MANE Select ENSP00000324532.8:p.Lys2759Asn
ENST00000649721.1:c.4872G>C ENSP00000497885.1:p.Lys1624Asn
ENST00000269217.10:c.3450G>C ENSP00000269217.5:p.Lys1150Asn
ENST00000313654.13:c.8277G>C ENSP00000324532.8:p.Lys2759Asn
ENST00000399516.7:c.8109G>C ENSP00000382432.2:p.Lys2703Asn
ENST00000586751.5:c.3055G>C
ENST00000587184.5:c.3282G>C ENSP00000466557.1:p.Lys1094Asn
ENST00000588770.5:n.2855G>C
NM_000227.4:c.3450G>C NP_000218.3:p.Lys1150Asn
NM_001127717.2:c.8109G>C NP_001121189.2:p.Lys2703Asn
NM_001127718.2:c.3282G>C NP_001121190.2:p.Lys1094Asn
NM_198129.2:c.8277G>C NP_937762.2:p.Lys2759Asn
XM_011525978.1:c.8304G>C XP_011524280.1:p.Lys2768Asn
XM_011525979.1:c.8295G>C XP_011524281.1:p.Lys2765Asn
XM_011525980.1:c.8286G>C XP_011524282.1:p.Lys2762Asn
XM_011525981.1:c.8172G>C XP_011524283.1:p.Lys2724Asn
XM_011525982.1:c.8007G>C XP_011524284.1:p.Lys2669Asn
XM_011525978.2:c.8304G>C XP_011524280.1:p.Lys2768Asn
XM_011525979.2:c.8295G>C XP_011524281.1:p.Lys2765Asn
XM_011525980.2:c.8286G>C XP_011524282.1:p.Lys2762Asn
XM_011525981.2:c.8172G>C XP_011524283.1:p.Lys2724Asn
XM_011525982.2:c.8007G>C XP_011524284.1:p.Lys2669Asn
XM_017025743.1:c.6156G>C XP_016881232.1:p.Lys2052Asn
XM_017025744.1:c.3846G>C XP_016881233.1:p.Lys1282Asn
XR_001753199.1:n.8545G>C
NM_000227.5:c.3450G>C NP_000218.3:p.Lys1150Asn
NM_001127717.3:c.8109G>C NP_001121189.2:p.Lys2703Asn
NM_001127718.3:c.3282G>C NP_001121190.2:p.Lys1094Asn
NM_198129.3:c.8277G>C NP_937762.2:p.Lys2759Asn
NM_000227.6:c.3450G>C MANE Plus Clinical NP_000218.3:p.Lys1150Asn
NM_001127717.4:c.8109G>C NP_001121189.2:p.Lys2703Asn
NM_001127718.4:c.3282G>C NP_001121190.2:p.Lys1094Asn
NM_198129.4:c.8277G>C MANE Select NP_937762.2:p.Lys2759Asn