Canonical Allele Identifier: CA402063326
Gene: LAMA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23928218A>T , CM000680.2:g.23928218A>T GRCh38
NC_000018.9:g.21508182A>T , CM000680.1:g.21508182A>T GRCh37
NC_000018.8:g.19762180A>T NCBI36
NG_007853.2:g.243621A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000269217.11:c.3446A>T MANE Plus Clinical ENSP00000269217.5:p.Lys1149Ile
ENST00000313654.14:c.8273A>T MANE Select ENSP00000324532.8:p.Lys2758Ile
ENST00000649721.1:c.4868A>T ENSP00000497885.1:p.Lys1623Ile
ENST00000269217.10:c.3446A>T ENSP00000269217.5:p.Lys1149Ile
ENST00000313654.13:c.8273A>T ENSP00000324532.8:p.Lys2758Ile
ENST00000399516.7:c.8105A>T ENSP00000382432.2:p.Lys2702Ile
ENST00000586751.5:c.3051A>T
ENST00000587184.5:c.3278A>T ENSP00000466557.1:p.Lys1093Ile
ENST00000588770.5:n.2851A>T
NM_000227.4:c.3446A>T NP_000218.3:p.Lys1149Ile
NM_001127717.2:c.8105A>T NP_001121189.2:p.Lys2702Ile
NM_001127718.2:c.3278A>T NP_001121190.2:p.Lys1093Ile
NM_198129.2:c.8273A>T NP_937762.2:p.Lys2758Ile
XM_011525978.1:c.8300A>T XP_011524280.1:p.Lys2767Ile
XM_011525979.1:c.8291A>T XP_011524281.1:p.Lys2764Ile
XM_011525980.1:c.8282A>T XP_011524282.1:p.Lys2761Ile
XM_011525981.1:c.8168A>T XP_011524283.1:p.Lys2723Ile
XM_011525982.1:c.8003A>T XP_011524284.1:p.Lys2668Ile
XM_011525978.2:c.8300A>T XP_011524280.1:p.Lys2767Ile
XM_011525979.2:c.8291A>T XP_011524281.1:p.Lys2764Ile
XM_011525980.2:c.8282A>T XP_011524282.1:p.Lys2761Ile
XM_011525981.2:c.8168A>T XP_011524283.1:p.Lys2723Ile
XM_011525982.2:c.8003A>T XP_011524284.1:p.Lys2668Ile
XM_017025743.1:c.6152A>T XP_016881232.1:p.Lys2051Ile
XM_017025744.1:c.3842A>T XP_016881233.1:p.Lys1281Ile
XR_001753199.1:n.8541A>T
NM_000227.5:c.3446A>T NP_000218.3:p.Lys1149Ile
NM_001127717.3:c.8105A>T NP_001121189.2:p.Lys2702Ile
NM_001127718.3:c.3278A>T NP_001121190.2:p.Lys1093Ile
NM_198129.3:c.8273A>T NP_937762.2:p.Lys2758Ile
NM_000227.6:c.3446A>T MANE Plus Clinical NP_000218.3:p.Lys1149Ile
NM_001127717.4:c.8105A>T NP_001121189.2:p.Lys2702Ile
NM_001127718.4:c.3278A>T NP_001121190.2:p.Lys1093Ile
NM_198129.4:c.8273A>T MANE Select NP_937762.2:p.Lys2758Ile