Canonical Allele Identifier: CA402045085
Gene: LAMA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23876402T>G , CM000680.2:g.23876402T>G GRCh38
NC_000018.9:g.21456366T>G , CM000680.1:g.21456366T>G GRCh37
NC_000018.8:g.19710364T>G NCBI36
NG_007853.2:g.191805T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000269217.11:c.280T>G MANE Plus Clinical ENSP00000269217.5:p.Cys94Gly
ENST00000313654.14:c.5107T>G MANE Select ENSP00000324532.8:p.Cys1703Gly
ENST00000649721.1:c.1999T>G ENSP00000497885.1:p.Cys667Gly
ENST00000269217.10:c.280T>G ENSP00000269217.5:p.Cys94Gly
ENST00000313654.13:c.5107T>G ENSP00000324532.8:p.Cys1703Gly
ENST00000399516.7:c.5107T>G ENSP00000382432.2:p.Cys1703Gly
ENST00000587184.5:c.280T>G ENSP00000466557.1:p.Cys94Gly
NM_000227.4:c.280T>G NP_000218.3:p.Cys94Gly
NM_001127717.2:c.5107T>G NP_001121189.2:p.Cys1703Gly
NM_001127718.2:c.280T>G NP_001121190.2:p.Cys94Gly
NM_198129.2:c.5107T>G NP_937762.2:p.Cys1703Gly
XM_011525978.1:c.5134T>G XP_011524280.1:p.Cys1712Gly
XM_011525979.1:c.5125T>G XP_011524281.1:p.Cys1709Gly
XM_011525980.1:c.5116T>G XP_011524282.1:p.Cys1706Gly
XM_011525981.1:c.5002T>G XP_011524283.1:p.Cys1668Gly
XM_011525982.1:c.5134T>G XP_011524284.1:p.Cys1712Gly
XM_011525978.2:c.5134T>G XP_011524280.1:p.Cys1712Gly
XM_011525979.2:c.5125T>G XP_011524281.1:p.Cys1709Gly
XM_011525980.2:c.5116T>G XP_011524282.1:p.Cys1706Gly
XM_011525981.2:c.5002T>G XP_011524283.1:p.Cys1668Gly
XM_011525982.2:c.5134T>G XP_011524284.1:p.Cys1712Gly
XM_017025743.1:c.2986T>G XP_016881232.1:p.Cys996Gly
XM_017025744.1:c.676T>G XP_016881233.1:p.Cys226Gly
XR_001753199.1:n.5375T>G
NM_000227.5:c.280T>G NP_000218.3:p.Cys94Gly
NM_001127717.3:c.5107T>G NP_001121189.2:p.Cys1703Gly
NM_001127718.3:c.280T>G NP_001121190.2:p.Cys94Gly
NM_198129.3:c.5107T>G NP_937762.2:p.Cys1703Gly
NM_000227.6:c.280T>G MANE Plus Clinical NP_000218.3:p.Cys94Gly
NM_001127717.4:c.5107T>G NP_001121189.2:p.Cys1703Gly
NM_001127718.4:c.280T>G NP_001121190.2:p.Cys94Gly
NM_198129.4:c.5107T>G MANE Select NP_937762.2:p.Cys1703Gly