Canonical Allele Identifier: CA402059340

Gene: LAMA3

Linked Data

• dbSNP Id: rs1370758107
• gnomAD v2: 18-21495364-A-G
• MyVariant Identifiers: chr18:g.21495364A>G (hg19) ; chr18:g.23915400A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915400A>G , CM000680.2:g.23915400A>G	GRCh38
NC_000018.9:g.21495364A>G , CM000680.1:g.21495364A>G	GRCh37
NC_000018.8:g.19749362A>G	NCBI36
NG_007853.2:g.230803A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2929A>G MANE Plus Clinical	ENSP00000269217.5:p.Thr977Ala
ENST00000313654.14:c.7756A>G MANE Select	ENSP00000324532.8:p.Thr2586Ala
ENST00000649721.1:c.4351A>G	ENSP00000497885.1:p.Thr1451Ala
ENST00000269217.10:c.2929A>G	ENSP00000269217.5:p.Thr977Ala
ENST00000313654.13:c.7756A>G	ENSP00000324532.8:p.Thr2586Ala
ENST00000399516.7:c.7588A>G	ENSP00000382432.2:p.Thr2530Ala
ENST00000586751.5:c.2534A>G
ENST00000587184.5:c.2761A>G	ENSP00000466557.1:p.Thr921Ala
ENST00000588770.5:n.2334A>G
NM_000227.4:c.2929A>G	NP_000218.3:p.Thr977Ala
NM_001127717.2:c.7588A>G	NP_001121189.2:p.Thr2530Ala
NM_001127718.2:c.2761A>G	NP_001121190.2:p.Thr921Ala
NM_198129.2:c.7756A>G	NP_937762.2:p.Thr2586Ala
XM_011525978.1:c.7783A>G	XP_011524280.1:p.Thr2595Ala
XM_011525979.1:c.7774A>G	XP_011524281.1:p.Thr2592Ala
XM_011525980.1:c.7765A>G	XP_011524282.1:p.Thr2589Ala
XM_011525981.1:c.7651A>G	XP_011524283.1:p.Thr2551Ala
XM_011525982.1:c.7486A>G	XP_011524284.1:p.Thr2496Ala
XM_011525978.2:c.7783A>G	XP_011524280.1:p.Thr2595Ala
XM_011525979.2:c.7774A>G	XP_011524281.1:p.Thr2592Ala
XM_011525980.2:c.7765A>G	XP_011524282.1:p.Thr2589Ala
XM_011525981.2:c.7651A>G	XP_011524283.1:p.Thr2551Ala
XM_011525982.2:c.7486A>G	XP_011524284.1:p.Thr2496Ala
XM_017025743.1:c.5635A>G	XP_016881232.1:p.Thr1879Ala
XM_017025744.1:c.3325A>G	XP_016881233.1:p.Thr1109Ala
XR_001753199.1:n.8024A>G
NM_000227.5:c.2929A>G	NP_000218.3:p.Thr977Ala
NM_001127717.3:c.7588A>G	NP_001121189.2:p.Thr2530Ala
NM_001127718.3:c.2761A>G	NP_001121190.2:p.Thr921Ala
NM_198129.3:c.7756A>G	NP_937762.2:p.Thr2586Ala
NM_000227.6:c.2929A>G MANE Plus Clinical	NP_000218.3:p.Thr977Ala
NM_001127717.4:c.7588A>G	NP_001121189.2:p.Thr2530Ala
NM_001127718.4:c.2761A>G	NP_001121190.2:p.Thr921Ala
NM_198129.4:c.7756A>G MANE Select	NP_937762.2:p.Thr2586Ala