Canonical Allele Identifier: CA402051851

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21529886T>A (hg19) ; chr18:g.23949922T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23949922T>A , CM000680.2:g.23949922T>A	GRCh38
NC_000018.9:g.21529886T>A , CM000680.1:g.21529886T>A	GRCh37
NC_000018.8:g.19783884T>A	NCBI36
NG_007853.2:g.265325T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.4682T>A MANE Plus Clinical	ENSP00000269217.5:p.Leu1561Ter
ENST00000313654.14:c.9509T>A MANE Select	ENSP00000324532.8:p.Leu3170Ter
ENST00000649721.1:c.6104T>A	ENSP00000497885.1:p.Leu2035Ter
ENST00000269217.10:c.4682T>A	ENSP00000269217.5:p.Leu1561Ter
ENST00000313654.13:c.9509T>A	ENSP00000324532.8:p.Leu3170Ter
ENST00000399516.7:c.9341T>A	ENSP00000382432.2:p.Leu3114Ter
ENST00000587184.5:c.4514T>A	ENSP00000466557.1:p.Leu1505Ter
ENST00000588004.1:c.30T>A
ENST00000588770.5:n.4087T>A
NM_000227.4:c.4682T>A	NP_000218.3:p.Leu1561Ter
NM_001127717.2:c.9341T>A	NP_001121189.2:p.Leu3114Ter
NM_001127718.2:c.4514T>A	NP_001121190.2:p.Leu1505Ter
NM_198129.2:c.9509T>A	NP_937762.2:p.Leu3170Ter
XM_011525978.1:c.9536T>A	XP_011524280.1:p.Leu3179Ter
XM_011525979.1:c.9527T>A	XP_011524281.1:p.Leu3176Ter
XM_011525980.1:c.9518T>A	XP_011524282.1:p.Leu3173Ter
XM_011525981.1:c.9404T>A	XP_011524283.1:p.Leu3135Ter
XM_011525982.1:c.9239T>A	XP_011524284.1:p.Leu3080Ter
XM_011525978.2:c.9536T>A	XP_011524280.1:p.Leu3179Ter
XM_011525979.2:c.9527T>A	XP_011524281.1:p.Leu3176Ter
XM_011525980.2:c.9518T>A	XP_011524282.1:p.Leu3173Ter
XM_011525981.2:c.9404T>A	XP_011524283.1:p.Leu3135Ter
XM_011525982.2:c.9239T>A	XP_011524284.1:p.Leu3080Ter
XM_017025743.1:c.7388T>A	XP_016881232.1:p.Leu2463Ter
XM_017025744.1:c.5078T>A	XP_016881233.1:p.Leu1693Ter
XR_001753199.1:n.9777T>A
NM_000227.5:c.4682T>A	NP_000218.3:p.Leu1561Ter
NM_001127717.3:c.9341T>A	NP_001121189.2:p.Leu3114Ter
NM_001127718.3:c.4514T>A	NP_001121190.2:p.Leu1505Ter
NM_198129.3:c.9509T>A	NP_937762.2:p.Leu3170Ter
NM_000227.6:c.4682T>A MANE Plus Clinical	NP_000218.3:p.Leu1561Ter
NM_001127717.4:c.9341T>A	NP_001121189.2:p.Leu3114Ter
NM_001127718.4:c.4514T>A	NP_001121190.2:p.Leu1505Ter
NM_198129.4:c.9509T>A MANE Select	NP_937762.2:p.Leu3170Ter