Canonical Allele Identifier: CA402051303

Gene: LAMA3

Linked Data

• gnomAD v4: 18-23905539-T-A
• MyVariant Identifiers: chr18:g.21485503T>A (hg19) ; chr18:g.23905539T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23905539T>A , CM000680.2:g.23905539T>A	GRCh38
NC_000018.9:g.21485503T>A , CM000680.1:g.21485503T>A	GRCh37
NC_000018.8:g.19739501T>A	NCBI36
NG_007853.2:g.220942T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1806T>A MANE Plus Clinical	ENSP00000269217.5:p.Asp602Glu
ENST00000313654.14:c.6633T>A MANE Select	ENSP00000324532.8:p.Asp2211Glu
ENST00000649721.1:c.3525T>A	ENSP00000497885.1:p.Asp1175Glu
ENST00000269217.10:c.1806T>A	ENSP00000269217.5:p.Asp602Glu
ENST00000313654.13:c.6633T>A	ENSP00000324532.8:p.Asp2211Glu
ENST00000399516.7:c.6465T>A	ENSP00000382432.2:p.Asp2155Glu
ENST00000586751.5:c.1411T>A
ENST00000587184.5:c.1638T>A	ENSP00000466557.1:p.Asp546Glu
ENST00000588770.5:n.1211T>A
NM_000227.4:c.1806T>A	NP_000218.3:p.Asp602Glu
NM_001127717.2:c.6465T>A	NP_001121189.2:p.Asp2155Glu
NM_001127718.2:c.1638T>A	NP_001121190.2:p.Asp546Glu
NM_198129.2:c.6633T>A	NP_937762.2:p.Asp2211Glu
XM_011525978.1:c.6660T>A	XP_011524280.1:p.Asp2220Glu
XM_011525979.1:c.6651T>A	XP_011524281.1:p.Asp2217Glu
XM_011525980.1:c.6642T>A	XP_011524282.1:p.Asp2214Glu
XM_011525981.1:c.6528T>A	XP_011524283.1:p.Asp2176Glu
XM_011525982.1:c.6660T>A	XP_011524284.1:p.Asp2220Glu
XM_011525978.2:c.6660T>A	XP_011524280.1:p.Asp2220Glu
XM_011525979.2:c.6651T>A	XP_011524281.1:p.Asp2217Glu
XM_011525980.2:c.6642T>A	XP_011524282.1:p.Asp2214Glu
XM_011525981.2:c.6528T>A	XP_011524283.1:p.Asp2176Glu
XM_011525982.2:c.6660T>A	XP_011524284.1:p.Asp2220Glu
XM_017025743.1:c.4512T>A	XP_016881232.1:p.Asp1504Glu
XM_017025744.1:c.2202T>A	XP_016881233.1:p.Asp734Glu
XR_001753199.1:n.6901T>A
NM_000227.5:c.1806T>A	NP_000218.3:p.Asp602Glu
NM_001127717.3:c.6465T>A	NP_001121189.2:p.Asp2155Glu
NM_001127718.3:c.1638T>A	NP_001121190.2:p.Asp546Glu
NM_198129.3:c.6633T>A	NP_937762.2:p.Asp2211Glu
NM_000227.6:c.1806T>A MANE Plus Clinical	NP_000218.3:p.Asp602Glu
NM_001127717.4:c.6465T>A	NP_001121189.2:p.Asp2155Glu
NM_001127718.4:c.1638T>A	NP_001121190.2:p.Asp546Glu
NM_198129.4:c.6633T>A MANE Select	NP_937762.2:p.Asp2211Glu