Canonical Allele Identifier: CA402051291
Gene: LAMA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23905535A>C , CM000680.2:g.23905535A>C GRCh38
NC_000018.9:g.21485499A>C , CM000680.1:g.21485499A>C GRCh37
NC_000018.8:g.19739497A>C NCBI36
NG_007853.2:g.220938A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269217.11:c.1802A>C MANE Plus Clinical ENSP00000269217.5:p.Glu601Ala
ENST00000313654.14:c.6629A>C MANE Select ENSP00000324532.8:p.Glu2210Ala
ENST00000649721.1:c.3521A>C ENSP00000497885.1:p.Glu1174Ala
ENST00000269217.10:c.1802A>C ENSP00000269217.5:p.Glu601Ala
ENST00000313654.13:c.6629A>C ENSP00000324532.8:p.Glu2210Ala
ENST00000399516.7:c.6461A>C ENSP00000382432.2:p.Glu2154Ala
ENST00000586751.5:c.1407A>C
ENST00000587184.5:c.1634A>C ENSP00000466557.1:p.Glu545Ala
ENST00000588770.5:n.1207A>C
NM_000227.4:c.1802A>C NP_000218.3:p.Glu601Ala
NM_001127717.2:c.6461A>C NP_001121189.2:p.Glu2154Ala
NM_001127718.2:c.1634A>C NP_001121190.2:p.Glu545Ala
NM_198129.2:c.6629A>C NP_937762.2:p.Glu2210Ala
XM_011525978.1:c.6656A>C XP_011524280.1:p.Glu2219Ala
XM_011525979.1:c.6647A>C XP_011524281.1:p.Glu2216Ala
XM_011525980.1:c.6638A>C XP_011524282.1:p.Glu2213Ala
XM_011525981.1:c.6524A>C XP_011524283.1:p.Glu2175Ala
XM_011525982.1:c.6656A>C XP_011524284.1:p.Glu2219Ala
XM_011525978.2:c.6656A>C XP_011524280.1:p.Glu2219Ala
XM_011525979.2:c.6647A>C XP_011524281.1:p.Glu2216Ala
XM_011525980.2:c.6638A>C XP_011524282.1:p.Glu2213Ala
XM_011525981.2:c.6524A>C XP_011524283.1:p.Glu2175Ala
XM_011525982.2:c.6656A>C XP_011524284.1:p.Glu2219Ala
XM_017025743.1:c.4508A>C XP_016881232.1:p.Glu1503Ala
XM_017025744.1:c.2198A>C XP_016881233.1:p.Glu733Ala
XR_001753199.1:n.6897A>C
NM_000227.5:c.1802A>C NP_000218.3:p.Glu601Ala
NM_001127717.3:c.6461A>C NP_001121189.2:p.Glu2154Ala
NM_001127718.3:c.1634A>C NP_001121190.2:p.Glu545Ala
NM_198129.3:c.6629A>C NP_937762.2:p.Glu2210Ala
NM_000227.6:c.1802A>C MANE Plus Clinical NP_000218.3:p.Glu601Ala
NM_001127717.4:c.6461A>C NP_001121189.2:p.Glu2154Ala
NM_001127718.4:c.1634A>C NP_001121190.2:p.Glu545Ala
NM_198129.4:c.6629A>C MANE Select NP_937762.2:p.Glu2210Ala