Canonical Allele Identifier: CA402045081
Gene: LAMA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23876400T>G , CM000680.2:g.23876400T>G GRCh38
NC_000018.9:g.21456364T>G , CM000680.1:g.21456364T>G GRCh37
NC_000018.8:g.19710362T>G NCBI36
NG_007853.2:g.191803T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000269217.11:c.278T>G MANE Plus Clinical ENSP00000269217.5:p.Ile93Arg
ENST00000313654.14:c.5105T>G MANE Select ENSP00000324532.8:p.Ile1702Arg
ENST00000649721.1:c.1997T>G ENSP00000497885.1:p.Ile666Arg
ENST00000269217.10:c.278T>G ENSP00000269217.5:p.Ile93Arg
ENST00000313654.13:c.5105T>G ENSP00000324532.8:p.Ile1702Arg
ENST00000399516.7:c.5105T>G ENSP00000382432.2:p.Ile1702Arg
ENST00000587184.5:c.278T>G ENSP00000466557.1:p.Ile93Arg
NM_000227.4:c.278T>G NP_000218.3:p.Ile93Arg
NM_001127717.2:c.5105T>G NP_001121189.2:p.Ile1702Arg
NM_001127718.2:c.278T>G NP_001121190.2:p.Ile93Arg
NM_198129.2:c.5105T>G NP_937762.2:p.Ile1702Arg
XM_011525978.1:c.5132T>G XP_011524280.1:p.Ile1711Arg
XM_011525979.1:c.5123T>G XP_011524281.1:p.Ile1708Arg
XM_011525980.1:c.5114T>G XP_011524282.1:p.Ile1705Arg
XM_011525981.1:c.5000T>G XP_011524283.1:p.Ile1667Arg
XM_011525982.1:c.5132T>G XP_011524284.1:p.Ile1711Arg
XM_011525978.2:c.5132T>G XP_011524280.1:p.Ile1711Arg
XM_011525979.2:c.5123T>G XP_011524281.1:p.Ile1708Arg
XM_011525980.2:c.5114T>G XP_011524282.1:p.Ile1705Arg
XM_011525981.2:c.5000T>G XP_011524283.1:p.Ile1667Arg
XM_011525982.2:c.5132T>G XP_011524284.1:p.Ile1711Arg
XM_017025743.1:c.2984T>G XP_016881232.1:p.Ile995Arg
XM_017025744.1:c.674T>G XP_016881233.1:p.Ile225Arg
XR_001753199.1:n.5373T>G
NM_000227.5:c.278T>G NP_000218.3:p.Ile93Arg
NM_001127717.3:c.5105T>G NP_001121189.2:p.Ile1702Arg
NM_001127718.3:c.278T>G NP_001121190.2:p.Ile93Arg
NM_198129.3:c.5105T>G NP_937762.2:p.Ile1702Arg
NM_000227.6:c.278T>G MANE Plus Clinical NP_000218.3:p.Ile93Arg
NM_001127717.4:c.5105T>G NP_001121189.2:p.Ile1702Arg
NM_001127718.4:c.278T>G NP_001121190.2:p.Ile93Arg
NM_198129.4:c.5105T>G MANE Select NP_937762.2:p.Ile1702Arg