Canonical Allele Identifier: CA503339730

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21495384A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915420A>G , CM000680.2:g.23915420A>G	GRCh38
NC_000018.9:g.21495384A>G , CM000680.1:g.21495384A>G	GRCh37
NC_000018.8:g.19749382A>G	NCBI36
NG_007853.2:g.230823A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2949A>G MANE Plus Clinical	ENSP00000269217.5:p.Arg983=
ENST00000313654.14:c.7776A>G MANE Select	ENSP00000324532.8:p.Arg2592=
ENST00000649721.1:c.4371A>G	ENSP00000497885.1:p.Arg1457=
ENST00000269217.10:c.2949A>G	ENSP00000269217.5:p.Arg983=
ENST00000313654.13:c.7776A>G	ENSP00000324532.8:p.Arg2592=
ENST00000399516.7:c.7608A>G	ENSP00000382432.2:p.Arg2536=
ENST00000586751.5:c.2554A>G
ENST00000587184.5:c.2781A>G	ENSP00000466557.1:p.Arg927=
ENST00000588770.5:n.2354A>G
NM_000227.4:c.2949A>G	NP_000218.3:p.Arg983=
NM_001127717.2:c.7608A>G	NP_001121189.2:p.Arg2536=
NM_001127718.2:c.2781A>G	NP_001121190.2:p.Arg927=
NM_198129.2:c.7776A>G	NP_937762.2:p.Arg2592=
XM_011525978.1:c.7803A>G	XP_011524280.1:p.Arg2601=
XM_011525979.1:c.7794A>G	XP_011524281.1:p.Arg2598=
XM_011525980.1:c.7785A>G	XP_011524282.1:p.Arg2595=
XM_011525981.1:c.7671A>G	XP_011524283.1:p.Arg2557=
XM_011525982.1:c.7506A>G	XP_011524284.1:p.Arg2502=
XM_011525978.2:c.7803A>G	XP_011524280.1:p.Arg2601=
XM_011525979.2:c.7794A>G	XP_011524281.1:p.Arg2598=
XM_011525980.2:c.7785A>G	XP_011524282.1:p.Arg2595=
XM_011525981.2:c.7671A>G	XP_011524283.1:p.Arg2557=
XM_011525982.2:c.7506A>G	XP_011524284.1:p.Arg2502=
XM_017025743.1:c.5655A>G	XP_016881232.1:p.Arg1885=
XM_017025744.1:c.3345A>G	XP_016881233.1:p.Arg1115=
XR_001753199.1:n.8044A>G
NM_000227.5:c.2949A>G	NP_000218.3:p.Arg983=
NM_001127717.3:c.7608A>G	NP_001121189.2:p.Arg2536=
NM_001127718.3:c.2781A>G	NP_001121190.2:p.Arg927=
NM_198129.3:c.7776A>G	NP_937762.2:p.Arg2592=
NM_000227.6:c.2949A>G MANE Plus Clinical	NP_000218.3:p.Arg983=
NM_001127717.4:c.7608A>G	NP_001121189.2:p.Arg2536=
NM_001127718.4:c.2781A>G	NP_001121190.2:p.Arg927=
NM_198129.4:c.7776A>G MANE Select	NP_937762.2:p.Arg2592=