Canonical Allele Identifier: CA503334996

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21483053C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23903089C>G , CM000680.2:g.23903089C>G	GRCh38
NC_000018.9:g.21483053C>G , CM000680.1:g.21483053C>G	GRCh37
NC_000018.8:g.19737051C>G	NCBI36
NG_007853.2:g.218492C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1455C>G MANE Plus Clinical	ENSP00000269217.5:p.Thr485=
ENST00000313654.14:c.6282C>G MANE Select	ENSP00000324532.8:p.Thr2094=
ENST00000649721.1:c.3174C>G	ENSP00000497885.1:p.Thr1058=
ENST00000269217.10:c.1455C>G	ENSP00000269217.5:p.Thr485=
ENST00000313654.13:c.6282C>G	ENSP00000324532.8:p.Thr2094=
ENST00000399516.7:c.6114C>G	ENSP00000382432.2:p.Thr2038=
ENST00000586751.5:c.1060C>G
ENST00000587184.5:c.1287C>G	ENSP00000466557.1:p.Thr429=
ENST00000588770.5:n.860C>G
NM_000227.4:c.1455C>G	NP_000218.3:p.Thr485=
NM_001127717.2:c.6114C>G	NP_001121189.2:p.Thr2038=
NM_001127718.2:c.1287C>G	NP_001121190.2:p.Thr429=
NM_198129.2:c.6282C>G	NP_937762.2:p.Thr2094=
XM_011525978.1:c.6309C>G	XP_011524280.1:p.Thr2103=
XM_011525979.1:c.6300C>G	XP_011524281.1:p.Thr2100=
XM_011525980.1:c.6291C>G	XP_011524282.1:p.Thr2097=
XM_011525981.1:c.6177C>G	XP_011524283.1:p.Thr2059=
XM_011525982.1:c.6309C>G	XP_011524284.1:p.Thr2103=
XM_011525978.2:c.6309C>G	XP_011524280.1:p.Thr2103=
XM_011525979.2:c.6300C>G	XP_011524281.1:p.Thr2100=
XM_011525980.2:c.6291C>G	XP_011524282.1:p.Thr2097=
XM_011525981.2:c.6177C>G	XP_011524283.1:p.Thr2059=
XM_011525982.2:c.6309C>G	XP_011524284.1:p.Thr2103=
XM_017025743.1:c.4161C>G	XP_016881232.1:p.Thr1387=
XM_017025744.1:c.1851C>G	XP_016881233.1:p.Thr617=
XR_001753199.1:n.6550C>G
NM_000227.5:c.1455C>G	NP_000218.3:p.Thr485=
NM_001127717.3:c.6114C>G	NP_001121189.2:p.Thr2038=
NM_001127718.3:c.1287C>G	NP_001121190.2:p.Thr429=
NM_198129.3:c.6282C>G	NP_937762.2:p.Thr2094=
NM_000227.6:c.1455C>G MANE Plus Clinical	NP_000218.3:p.Thr485=
NM_001127717.4:c.6114C>G	NP_001121189.2:p.Thr2038=
NM_001127718.4:c.1287C>G	NP_001121190.2:p.Thr429=
NM_198129.4:c.6282C>G MANE Select	NP_937762.2:p.Thr2094=