Canonical Allele Identifier: CA402059334

Gene: LAMA3

Linked Data

• dbSNP Id: rs1306931123
• gnomAD v2: 18-21495361-A-G
• gnomAD v4: 18-23915397-A-G
• MyVariant Identifiers: chr18:g.21495361A>G (hg19) ; chr18:g.23915397A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915397A>G , CM000680.2:g.23915397A>G	GRCh38
NC_000018.9:g.21495361A>G , CM000680.1:g.21495361A>G	GRCh37
NC_000018.8:g.19749359A>G	NCBI36
NG_007853.2:g.230800A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2926A>G MANE Plus Clinical	ENSP00000269217.5:p.Thr976Ala
ENST00000313654.14:c.7753A>G MANE Select	ENSP00000324532.8:p.Thr2585Ala
ENST00000649721.1:c.4348A>G	ENSP00000497885.1:p.Thr1450Ala
ENST00000269217.10:c.2926A>G	ENSP00000269217.5:p.Thr976Ala
ENST00000313654.13:c.7753A>G	ENSP00000324532.8:p.Thr2585Ala
ENST00000399516.7:c.7585A>G	ENSP00000382432.2:p.Thr2529Ala
ENST00000586751.5:c.2531A>G
ENST00000587184.5:c.2758A>G	ENSP00000466557.1:p.Thr920Ala
ENST00000588770.5:n.2331A>G
NM_000227.4:c.2926A>G	NP_000218.3:p.Thr976Ala
NM_001127717.2:c.7585A>G	NP_001121189.2:p.Thr2529Ala
NM_001127718.2:c.2758A>G	NP_001121190.2:p.Thr920Ala
NM_198129.2:c.7753A>G	NP_937762.2:p.Thr2585Ala
XM_011525978.1:c.7780A>G	XP_011524280.1:p.Thr2594Ala
XM_011525979.1:c.7771A>G	XP_011524281.1:p.Thr2591Ala
XM_011525980.1:c.7762A>G	XP_011524282.1:p.Thr2588Ala
XM_011525981.1:c.7648A>G	XP_011524283.1:p.Thr2550Ala
XM_011525982.1:c.7483A>G	XP_011524284.1:p.Thr2495Ala
XM_011525978.2:c.7780A>G	XP_011524280.1:p.Thr2594Ala
XM_011525979.2:c.7771A>G	XP_011524281.1:p.Thr2591Ala
XM_011525980.2:c.7762A>G	XP_011524282.1:p.Thr2588Ala
XM_011525981.2:c.7648A>G	XP_011524283.1:p.Thr2550Ala
XM_011525982.2:c.7483A>G	XP_011524284.1:p.Thr2495Ala
XM_017025743.1:c.5632A>G	XP_016881232.1:p.Thr1878Ala
XM_017025744.1:c.3322A>G	XP_016881233.1:p.Thr1108Ala
XR_001753199.1:n.8021A>G
NM_000227.5:c.2926A>G	NP_000218.3:p.Thr976Ala
NM_001127717.3:c.7585A>G	NP_001121189.2:p.Thr2529Ala
NM_001127718.3:c.2758A>G	NP_001121190.2:p.Thr920Ala
NM_198129.3:c.7753A>G	NP_937762.2:p.Thr2585Ala
NM_000227.6:c.2926A>G MANE Plus Clinical	NP_000218.3:p.Thr976Ala
NM_001127717.4:c.7585A>G	NP_001121189.2:p.Thr2529Ala
NM_001127718.4:c.2758A>G	NP_001121190.2:p.Thr920Ala
NM_198129.4:c.7753A>G MANE Select	NP_937762.2:p.Thr2585Ala