Canonical Allele Identifier: CA402063511
Gene: LAMA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23928240G>C , CM000680.2:g.23928240G>C GRCh38
NC_000018.9:g.21508204G>C , CM000680.1:g.21508204G>C GRCh37
NC_000018.8:g.19762202G>C NCBI36
NG_007853.2:g.243643G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269217.11:c.3468G>C MANE Plus Clinical ENSP00000269217.5:p.Lys1156Asn
ENST00000313654.14:c.8295G>C MANE Select ENSP00000324532.8:p.Lys2765Asn
ENST00000649721.1:c.4890G>C ENSP00000497885.1:p.Lys1630Asn
ENST00000269217.10:c.3468G>C ENSP00000269217.5:p.Lys1156Asn
ENST00000313654.13:c.8295G>C ENSP00000324532.8:p.Lys2765Asn
ENST00000399516.7:c.8127G>C ENSP00000382432.2:p.Lys2709Asn
ENST00000586751.5:c.3073G>C
ENST00000587184.5:c.3300G>C ENSP00000466557.1:p.Lys1100Asn
ENST00000588770.5:n.2873G>C
NM_000227.4:c.3468G>C NP_000218.3:p.Lys1156Asn
NM_001127717.2:c.8127G>C NP_001121189.2:p.Lys2709Asn
NM_001127718.2:c.3300G>C NP_001121190.2:p.Lys1100Asn
NM_198129.2:c.8295G>C NP_937762.2:p.Lys2765Asn
XM_011525978.1:c.8322G>C XP_011524280.1:p.Lys2774Asn
XM_011525979.1:c.8313G>C XP_011524281.1:p.Lys2771Asn
XM_011525980.1:c.8304G>C XP_011524282.1:p.Lys2768Asn
XM_011525981.1:c.8190G>C XP_011524283.1:p.Lys2730Asn
XM_011525982.1:c.8025G>C XP_011524284.1:p.Lys2675Asn
XM_011525978.2:c.8322G>C XP_011524280.1:p.Lys2774Asn
XM_011525979.2:c.8313G>C XP_011524281.1:p.Lys2771Asn
XM_011525980.2:c.8304G>C XP_011524282.1:p.Lys2768Asn
XM_011525981.2:c.8190G>C XP_011524283.1:p.Lys2730Asn
XM_011525982.2:c.8025G>C XP_011524284.1:p.Lys2675Asn
XM_017025743.1:c.6174G>C XP_016881232.1:p.Lys2058Asn
XM_017025744.1:c.3864G>C XP_016881233.1:p.Lys1288Asn
XR_001753199.1:n.8563G>C
NM_000227.5:c.3468G>C NP_000218.3:p.Lys1156Asn
NM_001127717.3:c.8127G>C NP_001121189.2:p.Lys2709Asn
NM_001127718.3:c.3300G>C NP_001121190.2:p.Lys1100Asn
NM_198129.3:c.8295G>C NP_937762.2:p.Lys2765Asn
NM_000227.6:c.3468G>C MANE Plus Clinical NP_000218.3:p.Lys1156Asn
NM_001127717.4:c.8127G>C NP_001121189.2:p.Lys2709Asn
NM_001127718.4:c.3300G>C NP_001121190.2:p.Lys1100Asn
NM_198129.4:c.8295G>C MANE Select NP_937762.2:p.Lys2765Asn