Canonical Allele Identifier: CA402064442

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21511027C>G (hg19) ; chr18:g.23931063C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23931063C>G , CM000680.2:g.23931063C>G	GRCh38
NC_000018.9:g.21511027C>G , CM000680.1:g.21511027C>G	GRCh37
NC_000018.8:g.19765025C>G	NCBI36
NG_007853.2:g.246466C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3611C>G MANE Plus Clinical	ENSP00000269217.5:p.Thr1204Arg
ENST00000313654.14:c.8438C>G MANE Select	ENSP00000324532.8:p.Thr2813Arg
ENST00000649721.1:c.5033C>G	ENSP00000497885.1:p.Thr1678Arg
ENST00000269217.10:c.3611C>G	ENSP00000269217.5:p.Thr1204Arg
ENST00000313654.13:c.8438C>G	ENSP00000324532.8:p.Thr2813Arg
ENST00000399516.7:c.8270C>G	ENSP00000382432.2:p.Thr2757Arg
ENST00000586751.5:c.3216C>G
ENST00000587184.5:c.3443C>G	ENSP00000466557.1:p.Thr1148Arg
ENST00000588164.2:c.143C>G	ENSP00000467473.2:p.Thr48Arg
ENST00000588770.5:n.3016C>G
NM_000227.4:c.3611C>G	NP_000218.3:p.Thr1204Arg
NM_001127717.2:c.8270C>G	NP_001121189.2:p.Thr2757Arg
NM_001127718.2:c.3443C>G	NP_001121190.2:p.Thr1148Arg
NM_198129.2:c.8438C>G	NP_937762.2:p.Thr2813Arg
XM_011525978.1:c.8465C>G	XP_011524280.1:p.Thr2822Arg
XM_011525979.1:c.8456C>G	XP_011524281.1:p.Thr2819Arg
XM_011525980.1:c.8447C>G	XP_011524282.1:p.Thr2816Arg
XM_011525981.1:c.8333C>G	XP_011524283.1:p.Thr2778Arg
XM_011525982.1:c.8168C>G	XP_011524284.1:p.Thr2723Arg
XM_011525978.2:c.8465C>G	XP_011524280.1:p.Thr2822Arg
XM_011525979.2:c.8456C>G	XP_011524281.1:p.Thr2819Arg
XM_011525980.2:c.8447C>G	XP_011524282.1:p.Thr2816Arg
XM_011525981.2:c.8333C>G	XP_011524283.1:p.Thr2778Arg
XM_011525982.2:c.8168C>G	XP_011524284.1:p.Thr2723Arg
XM_017025743.1:c.6317C>G	XP_016881232.1:p.Thr2106Arg
XM_017025744.1:c.4007C>G	XP_016881233.1:p.Thr1336Arg
XR_001753199.1:n.8706C>G
NM_000227.5:c.3611C>G	NP_000218.3:p.Thr1204Arg
NM_001127717.3:c.8270C>G	NP_001121189.2:p.Thr2757Arg
NM_001127718.3:c.3443C>G	NP_001121190.2:p.Thr1148Arg
NM_198129.3:c.8438C>G	NP_937762.2:p.Thr2813Arg
NM_000227.6:c.3611C>G MANE Plus Clinical	NP_000218.3:p.Thr1204Arg
NM_001127717.4:c.8270C>G	NP_001121189.2:p.Thr2757Arg
NM_001127718.4:c.3443C>G	NP_001121190.2:p.Thr1148Arg
NM_198129.4:c.8438C>G MANE Select	NP_937762.2:p.Thr2813Arg