Canonical Allele Identifier: CA402045092
Gene: LAMA3 HGNC NCBI

Linked Data

dbSNP Id: rs2144863220

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23876405G>T , CM000680.2:g.23876405G>T GRCh38
NC_000018.9:g.21456369G>T , CM000680.1:g.21456369G>T GRCh37
NC_000018.8:g.19710367G>T NCBI36
NG_007853.2:g.191808G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000269217.11:c.283G>T MANE Plus Clinical ENSP00000269217.5:p.Val95Phe
ENST00000313654.14:c.5110G>T MANE Select ENSP00000324532.8:p.Val1704Phe
ENST00000649721.1:c.2002G>T ENSP00000497885.1:p.Val668Phe
ENST00000269217.10:c.283G>T ENSP00000269217.5:p.Val95Phe
ENST00000313654.13:c.5110G>T ENSP00000324532.8:p.Val1704Phe
ENST00000399516.7:c.5110G>T ENSP00000382432.2:p.Val1704Phe
ENST00000587184.5:c.283G>T ENSP00000466557.1:p.Val95Phe
NM_000227.4:c.283G>T NP_000218.3:p.Val95Phe
NM_001127717.2:c.5110G>T NP_001121189.2:p.Val1704Phe
NM_001127718.2:c.283G>T NP_001121190.2:p.Val95Phe
NM_198129.2:c.5110G>T NP_937762.2:p.Val1704Phe
XM_011525978.1:c.5137G>T XP_011524280.1:p.Val1713Phe
XM_011525979.1:c.5128G>T XP_011524281.1:p.Val1710Phe
XM_011525980.1:c.5119G>T XP_011524282.1:p.Val1707Phe
XM_011525981.1:c.5005G>T XP_011524283.1:p.Val1669Phe
XM_011525982.1:c.5137G>T XP_011524284.1:p.Val1713Phe
XM_011525978.2:c.5137G>T XP_011524280.1:p.Val1713Phe
XM_011525979.2:c.5128G>T XP_011524281.1:p.Val1710Phe
XM_011525980.2:c.5119G>T XP_011524282.1:p.Val1707Phe
XM_011525981.2:c.5005G>T XP_011524283.1:p.Val1669Phe
XM_011525982.2:c.5137G>T XP_011524284.1:p.Val1713Phe
XM_017025743.1:c.2989G>T XP_016881232.1:p.Val997Phe
XM_017025744.1:c.679G>T XP_016881233.1:p.Val227Phe
XR_001753199.1:n.5378G>T
NM_000227.5:c.283G>T NP_000218.3:p.Val95Phe
NM_001127717.3:c.5110G>T NP_001121189.2:p.Val1704Phe
NM_001127718.3:c.283G>T NP_001121190.2:p.Val95Phe
NM_198129.3:c.5110G>T NP_937762.2:p.Val1704Phe
NM_000227.6:c.283G>T MANE Plus Clinical NP_000218.3:p.Val95Phe
NM_001127717.4:c.5110G>T NP_001121189.2:p.Val1704Phe
NM_001127718.4:c.283G>T NP_001121190.2:p.Val95Phe
NM_198129.4:c.5110G>T MANE Select NP_937762.2:p.Val1704Phe