Canonical Allele Identifier: CA402063135
Gene: LAMA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23928178A>G , CM000680.2:g.23928178A>G GRCh38
NC_000018.9:g.21508142A>G , CM000680.1:g.21508142A>G GRCh37
NC_000018.8:g.19762140A>G NCBI36
NG_007853.2:g.243581A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269217.11:c.3406A>G MANE Plus Clinical ENSP00000269217.5:p.Ser1136Gly
ENST00000313654.14:c.8233A>G MANE Select ENSP00000324532.8:p.Ser2745Gly
ENST00000649721.1:c.4828A>G ENSP00000497885.1:p.Ser1610Gly
ENST00000269217.10:c.3406A>G ENSP00000269217.5:p.Ser1136Gly
ENST00000313654.13:c.8233A>G ENSP00000324532.8:p.Ser2745Gly
ENST00000399516.7:c.8065A>G ENSP00000382432.2:p.Ser2689Gly
ENST00000586751.5:c.3011A>G
ENST00000587184.5:c.3238A>G ENSP00000466557.1:p.Ser1080Gly
ENST00000588770.5:n.2811A>G
NM_000227.4:c.3406A>G NP_000218.3:p.Ser1136Gly
NM_001127717.2:c.8065A>G NP_001121189.2:p.Ser2689Gly
NM_001127718.2:c.3238A>G NP_001121190.2:p.Ser1080Gly
NM_198129.2:c.8233A>G NP_937762.2:p.Ser2745Gly
XM_011525978.1:c.8260A>G XP_011524280.1:p.Ser2754Gly
XM_011525979.1:c.8251A>G XP_011524281.1:p.Ser2751Gly
XM_011525980.1:c.8242A>G XP_011524282.1:p.Ser2748Gly
XM_011525981.1:c.8128A>G XP_011524283.1:p.Ser2710Gly
XM_011525982.1:c.7963A>G XP_011524284.1:p.Ser2655Gly
XM_011525978.2:c.8260A>G XP_011524280.1:p.Ser2754Gly
XM_011525979.2:c.8251A>G XP_011524281.1:p.Ser2751Gly
XM_011525980.2:c.8242A>G XP_011524282.1:p.Ser2748Gly
XM_011525981.2:c.8128A>G XP_011524283.1:p.Ser2710Gly
XM_011525982.2:c.7963A>G XP_011524284.1:p.Ser2655Gly
XM_017025743.1:c.6112A>G XP_016881232.1:p.Ser2038Gly
XM_017025744.1:c.3802A>G XP_016881233.1:p.Ser1268Gly
XR_001753199.1:n.8501A>G
NM_000227.5:c.3406A>G NP_000218.3:p.Ser1136Gly
NM_001127717.3:c.8065A>G NP_001121189.2:p.Ser2689Gly
NM_001127718.3:c.3238A>G NP_001121190.2:p.Ser1080Gly
NM_198129.3:c.8233A>G NP_937762.2:p.Ser2745Gly
NM_000227.6:c.3406A>G MANE Plus Clinical NP_000218.3:p.Ser1136Gly
NM_001127717.4:c.8065A>G NP_001121189.2:p.Ser2689Gly
NM_001127718.4:c.3238A>G NP_001121190.2:p.Ser1080Gly
NM_198129.4:c.8233A>G MANE Select NP_937762.2:p.Ser2745Gly