Canonical Allele Identifier: CA402053022
Gene: LAMA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23907766T>A , CM000680.2:g.23907766T>A GRCh38
NC_000018.9:g.21487730T>A , CM000680.1:g.21487730T>A GRCh37
NC_000018.8:g.19741728T>A NCBI36
NG_007853.2:g.223169T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000269217.11:c.2019T>A MANE Plus Clinical ENSP00000269217.5:p.Asp673Glu
ENST00000313654.14:c.6846T>A MANE Select ENSP00000324532.8:p.Asp2282Glu
ENST00000649721.1:c.3611-1387T>A ENSP00000497885.1:n.3611-1387T>A
ENST00000269217.10:c.2019T>A ENSP00000269217.5:p.Asp673Glu
ENST00000313654.13:c.6846T>A ENSP00000324532.8:p.Asp2282Glu
ENST00000399516.7:c.6678T>A ENSP00000382432.2:p.Asp2226Glu
ENST00000586751.5:c.1624T>A
ENST00000587184.5:c.1851T>A ENSP00000466557.1:p.Asp617Glu
ENST00000588770.5:n.1424T>A
NM_000227.4:c.2019T>A NP_000218.3:p.Asp673Glu
NM_001127717.2:c.6678T>A NP_001121189.2:p.Asp2226Glu
NM_001127718.2:c.1851T>A NP_001121190.2:p.Asp617Glu
NM_198129.2:c.6846T>A NP_937762.2:p.Asp2282Glu
XM_011525978.1:c.6873T>A XP_011524280.1:p.Asp2291Glu
XM_011525979.1:c.6864T>A XP_011524281.1:p.Asp2288Glu
XM_011525980.1:c.6855T>A XP_011524282.1:p.Asp2285Glu
XM_011525981.1:c.6741T>A XP_011524283.1:p.Asp2247Glu
XM_011525982.1:c.6746-1387T>A XP_011524284.1:n.6746-1387T>A
XM_011525978.2:c.6873T>A XP_011524280.1:p.Asp2291Glu
XM_011525979.2:c.6864T>A XP_011524281.1:p.Asp2288Glu
XM_011525980.2:c.6855T>A XP_011524282.1:p.Asp2285Glu
XM_011525981.2:c.6741T>A XP_011524283.1:p.Asp2247Glu
XM_011525982.2:c.6746-1387T>A XP_011524284.1:n.6746-1387T>A
XM_017025743.1:c.4725T>A XP_016881232.1:p.Asp1575Glu
XM_017025744.1:c.2415T>A XP_016881233.1:p.Asp805Glu
XR_001753199.1:n.7114T>A
NM_000227.5:c.2019T>A NP_000218.3:p.Asp673Glu
NM_001127717.3:c.6678T>A NP_001121189.2:p.Asp2226Glu
NM_001127718.3:c.1851T>A NP_001121190.2:p.Asp617Glu
NM_198129.3:c.6846T>A NP_937762.2:p.Asp2282Glu
NM_000227.6:c.2019T>A MANE Plus Clinical NP_000218.3:p.Asp673Glu
NM_001127717.4:c.6678T>A NP_001121189.2:p.Asp2226Glu
NM_001127718.4:c.1851T>A NP_001121190.2:p.Asp617Glu
NM_198129.4:c.6846T>A MANE Select NP_937762.2:p.Asp2282Glu