Canonical Allele Identifier: CA402044875
Gene: LAMA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23876306G>C , CM000680.2:g.23876306G>C GRCh38
NC_000018.9:g.21456270G>C , CM000680.1:g.21456270G>C GRCh37
NC_000018.8:g.19710268G>C NCBI36
NG_007853.2:g.191709G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000269217.11:c.184G>C MANE Plus Clinical ENSP00000269217.5:p.Gly62Arg
ENST00000313654.14:c.5011G>C MANE Select ENSP00000324532.8:p.Gly1671Arg
ENST00000649721.1:c.1903G>C ENSP00000497885.1:p.Gly635Arg
ENST00000269217.10:c.184G>C ENSP00000269217.5:p.Gly62Arg
ENST00000313654.13:c.5011G>C ENSP00000324532.8:p.Gly1671Arg
ENST00000399516.7:c.5011G>C ENSP00000382432.2:p.Gly1671Arg
ENST00000587184.5:c.184G>C ENSP00000466557.1:p.Gly62Arg
NM_000227.4:c.184G>C NP_000218.3:p.Gly62Arg
NM_001127717.2:c.5011G>C NP_001121189.2:p.Gly1671Arg
NM_001127718.2:c.184G>C NP_001121190.2:p.Gly62Arg
NM_198129.2:c.5011G>C NP_937762.2:p.Gly1671Arg
XM_011525978.1:c.5038G>C XP_011524280.1:p.Gly1680Arg
XM_011525979.1:c.5029G>C XP_011524281.1:p.Gly1677Arg
XM_011525980.1:c.5020G>C XP_011524282.1:p.Gly1674Arg
XM_011525981.1:c.4906G>C XP_011524283.1:p.Gly1636Arg
XM_011525982.1:c.5038G>C XP_011524284.1:p.Gly1680Arg
XM_011525978.2:c.5038G>C XP_011524280.1:p.Gly1680Arg
XM_011525979.2:c.5029G>C XP_011524281.1:p.Gly1677Arg
XM_011525980.2:c.5020G>C XP_011524282.1:p.Gly1674Arg
XM_011525981.2:c.4906G>C XP_011524283.1:p.Gly1636Arg
XM_011525982.2:c.5038G>C XP_011524284.1:p.Gly1680Arg
XM_017025743.1:c.2890G>C XP_016881232.1:p.Gly964Arg
XM_017025744.1:c.580G>C XP_016881233.1:p.Gly194Arg
XR_001753199.1:n.5279G>C
NM_000227.5:c.184G>C NP_000218.3:p.Gly62Arg
NM_001127717.3:c.5011G>C NP_001121189.2:p.Gly1671Arg
NM_001127718.3:c.184G>C NP_001121190.2:p.Gly62Arg
NM_198129.3:c.5011G>C NP_937762.2:p.Gly1671Arg
NM_000227.6:c.184G>C MANE Plus Clinical NP_000218.3:p.Gly62Arg
NM_001127717.4:c.5011G>C NP_001121189.2:p.Gly1671Arg
NM_001127718.4:c.184G>C NP_001121190.2:p.Gly62Arg
NM_198129.4:c.5011G>C MANE Select NP_937762.2:p.Gly1671Arg