Canonical Allele Identifier: CA402059367

Gene: LAMA3

Linked Data

• dbSNP Id: rs1876670881
• MyVariant Identifiers: chr18:g.21495376C>A (hg19) ; chr18:g.23915412C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915412C>A , CM000680.2:g.23915412C>A	GRCh38
NC_000018.9:g.21495376C>A , CM000680.1:g.21495376C>A	GRCh37
NC_000018.8:g.19749374C>A	NCBI36
NG_007853.2:g.230815C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2941C>A MANE Plus Clinical	ENSP00000269217.5:p.Pro981Thr
ENST00000313654.14:c.7768C>A MANE Select	ENSP00000324532.8:p.Pro2590Thr
ENST00000649721.1:c.4363C>A	ENSP00000497885.1:p.Pro1455Thr
ENST00000269217.10:c.2941C>A	ENSP00000269217.5:p.Pro981Thr
ENST00000313654.13:c.7768C>A	ENSP00000324532.8:p.Pro2590Thr
ENST00000399516.7:c.7600C>A	ENSP00000382432.2:p.Pro2534Thr
ENST00000586751.5:c.2546C>A
ENST00000587184.5:c.2773C>A	ENSP00000466557.1:p.Pro925Thr
ENST00000588770.5:n.2346C>A
NM_000227.4:c.2941C>A	NP_000218.3:p.Pro981Thr
NM_001127717.2:c.7600C>A	NP_001121189.2:p.Pro2534Thr
NM_001127718.2:c.2773C>A	NP_001121190.2:p.Pro925Thr
NM_198129.2:c.7768C>A	NP_937762.2:p.Pro2590Thr
XM_011525978.1:c.7795C>A	XP_011524280.1:p.Pro2599Thr
XM_011525979.1:c.7786C>A	XP_011524281.1:p.Pro2596Thr
XM_011525980.1:c.7777C>A	XP_011524282.1:p.Pro2593Thr
XM_011525981.1:c.7663C>A	XP_011524283.1:p.Pro2555Thr
XM_011525982.1:c.7498C>A	XP_011524284.1:p.Pro2500Thr
XM_011525978.2:c.7795C>A	XP_011524280.1:p.Pro2599Thr
XM_011525979.2:c.7786C>A	XP_011524281.1:p.Pro2596Thr
XM_011525980.2:c.7777C>A	XP_011524282.1:p.Pro2593Thr
XM_011525981.2:c.7663C>A	XP_011524283.1:p.Pro2555Thr
XM_011525982.2:c.7498C>A	XP_011524284.1:p.Pro2500Thr
XM_017025743.1:c.5647C>A	XP_016881232.1:p.Pro1883Thr
XM_017025744.1:c.3337C>A	XP_016881233.1:p.Pro1113Thr
XR_001753199.1:n.8036C>A
NM_000227.5:c.2941C>A	NP_000218.3:p.Pro981Thr
NM_001127717.3:c.7600C>A	NP_001121189.2:p.Pro2534Thr
NM_001127718.3:c.2773C>A	NP_001121190.2:p.Pro925Thr
NM_198129.3:c.7768C>A	NP_937762.2:p.Pro2590Thr
NM_000227.6:c.2941C>A MANE Plus Clinical	NP_000218.3:p.Pro981Thr
NM_001127717.4:c.7600C>A	NP_001121189.2:p.Pro2534Thr
NM_001127718.4:c.2773C>A	NP_001121190.2:p.Pro925Thr
NM_198129.4:c.7768C>A MANE Select	NP_937762.2:p.Pro2590Thr