Canonical Allele Identifier: CA402063505
Gene: LAMA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23928239A>T , CM000680.2:g.23928239A>T GRCh38
NC_000018.9:g.21508203A>T , CM000680.1:g.21508203A>T GRCh37
NC_000018.8:g.19762201A>T NCBI36
NG_007853.2:g.243642A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000269217.11:c.3467A>T MANE Plus Clinical ENSP00000269217.5:p.Lys1156Met
ENST00000313654.14:c.8294A>T MANE Select ENSP00000324532.8:p.Lys2765Met
ENST00000649721.1:c.4889A>T ENSP00000497885.1:p.Lys1630Met
ENST00000269217.10:c.3467A>T ENSP00000269217.5:p.Lys1156Met
ENST00000313654.13:c.8294A>T ENSP00000324532.8:p.Lys2765Met
ENST00000399516.7:c.8126A>T ENSP00000382432.2:p.Lys2709Met
ENST00000586751.5:c.3072A>T
ENST00000587184.5:c.3299A>T ENSP00000466557.1:p.Lys1100Met
ENST00000588770.5:n.2872A>T
NM_000227.4:c.3467A>T NP_000218.3:p.Lys1156Met
NM_001127717.2:c.8126A>T NP_001121189.2:p.Lys2709Met
NM_001127718.2:c.3299A>T NP_001121190.2:p.Lys1100Met
NM_198129.2:c.8294A>T NP_937762.2:p.Lys2765Met
XM_011525978.1:c.8321A>T XP_011524280.1:p.Lys2774Met
XM_011525979.1:c.8312A>T XP_011524281.1:p.Lys2771Met
XM_011525980.1:c.8303A>T XP_011524282.1:p.Lys2768Met
XM_011525981.1:c.8189A>T XP_011524283.1:p.Lys2730Met
XM_011525982.1:c.8024A>T XP_011524284.1:p.Lys2675Met
XM_011525978.2:c.8321A>T XP_011524280.1:p.Lys2774Met
XM_011525979.2:c.8312A>T XP_011524281.1:p.Lys2771Met
XM_011525980.2:c.8303A>T XP_011524282.1:p.Lys2768Met
XM_011525981.2:c.8189A>T XP_011524283.1:p.Lys2730Met
XM_011525982.2:c.8024A>T XP_011524284.1:p.Lys2675Met
XM_017025743.1:c.6173A>T XP_016881232.1:p.Lys2058Met
XM_017025744.1:c.3863A>T XP_016881233.1:p.Lys1288Met
XR_001753199.1:n.8562A>T
NM_000227.5:c.3467A>T NP_000218.3:p.Lys1156Met
NM_001127717.3:c.8126A>T NP_001121189.2:p.Lys2709Met
NM_001127718.3:c.3299A>T NP_001121190.2:p.Lys1100Met
NM_198129.3:c.8294A>T NP_937762.2:p.Lys2765Met
NM_000227.6:c.3467A>T MANE Plus Clinical NP_000218.3:p.Lys1156Met
NM_001127717.4:c.8126A>T NP_001121189.2:p.Lys2709Met
NM_001127718.4:c.3299A>T NP_001121190.2:p.Lys1100Met
NM_198129.4:c.8294A>T MANE Select NP_937762.2:p.Lys2765Met