Canonical Allele Identifier: CA402063298

Gene: LAMA3

Linked Data

• COSMIC: COSM5508759 ; COSM5508760
• MyVariant Identifiers: chr18:g.21508176T>G (hg19) ; chr18:g.23928212T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928212T>G , CM000680.2:g.23928212T>G	GRCh38
NC_000018.9:g.21508176T>G , CM000680.1:g.21508176T>G	GRCh37
NC_000018.8:g.19762174T>G	NCBI36
NG_007853.2:g.243615T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3440T>G MANE Plus Clinical	ENSP00000269217.5:p.Val1147Gly
ENST00000313654.14:c.8267T>G MANE Select	ENSP00000324532.8:p.Val2756Gly
ENST00000649721.1:c.4862T>G	ENSP00000497885.1:p.Val1621Gly
ENST00000269217.10:c.3440T>G	ENSP00000269217.5:p.Val1147Gly
ENST00000313654.13:c.8267T>G	ENSP00000324532.8:p.Val2756Gly
ENST00000399516.7:c.8099T>G	ENSP00000382432.2:p.Val2700Gly
ENST00000586751.5:c.3045T>G
ENST00000587184.5:c.3272T>G	ENSP00000466557.1:p.Val1091Gly
ENST00000588770.5:n.2845T>G
NM_000227.4:c.3440T>G	NP_000218.3:p.Val1147Gly
NM_001127717.2:c.8099T>G	NP_001121189.2:p.Val2700Gly
NM_001127718.2:c.3272T>G	NP_001121190.2:p.Val1091Gly
NM_198129.2:c.8267T>G	NP_937762.2:p.Val2756Gly
XM_011525978.1:c.8294T>G	XP_011524280.1:p.Val2765Gly
XM_011525979.1:c.8285T>G	XP_011524281.1:p.Val2762Gly
XM_011525980.1:c.8276T>G	XP_011524282.1:p.Val2759Gly
XM_011525981.1:c.8162T>G	XP_011524283.1:p.Val2721Gly
XM_011525982.1:c.7997T>G	XP_011524284.1:p.Val2666Gly
XM_011525978.2:c.8294T>G	XP_011524280.1:p.Val2765Gly
XM_011525979.2:c.8285T>G	XP_011524281.1:p.Val2762Gly
XM_011525980.2:c.8276T>G	XP_011524282.1:p.Val2759Gly
XM_011525981.2:c.8162T>G	XP_011524283.1:p.Val2721Gly
XM_011525982.2:c.7997T>G	XP_011524284.1:p.Val2666Gly
XM_017025743.1:c.6146T>G	XP_016881232.1:p.Val2049Gly
XM_017025744.1:c.3836T>G	XP_016881233.1:p.Val1279Gly
XR_001753199.1:n.8535T>G
NM_000227.5:c.3440T>G	NP_000218.3:p.Val1147Gly
NM_001127717.3:c.8099T>G	NP_001121189.2:p.Val2700Gly
NM_001127718.3:c.3272T>G	NP_001121190.2:p.Val1091Gly
NM_198129.3:c.8267T>G	NP_937762.2:p.Val2756Gly
NM_000227.6:c.3440T>G MANE Plus Clinical	NP_000218.3:p.Val1147Gly
NM_001127717.4:c.8099T>G	NP_001121189.2:p.Val2700Gly
NM_001127718.4:c.3272T>G	NP_001121190.2:p.Val1091Gly
NM_198129.4:c.8267T>G MANE Select	NP_937762.2:p.Val2756Gly