Canonical Allele Identifier: CA402059376

Gene: LAMA3

Linked Data

• COSMIC: COSM372884
• MyVariant Identifiers: chr18:g.21495380G>A (hg19) ; chr18:g.23915416G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915416G>A , CM000680.2:g.23915416G>A	GRCh38
NC_000018.9:g.21495380G>A , CM000680.1:g.21495380G>A	GRCh37
NC_000018.8:g.19749378G>A	NCBI36
NG_007853.2:g.230819G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2945G>A MANE Plus Clinical	ENSP00000269217.5:p.Cys982Tyr
ENST00000313654.14:c.7772G>A MANE Select	ENSP00000324532.8:p.Cys2591Tyr
ENST00000649721.1:c.4367G>A	ENSP00000497885.1:p.Cys1456Tyr
ENST00000269217.10:c.2945G>A	ENSP00000269217.5:p.Cys982Tyr
ENST00000313654.13:c.7772G>A	ENSP00000324532.8:p.Cys2591Tyr
ENST00000399516.7:c.7604G>A	ENSP00000382432.2:p.Cys2535Tyr
ENST00000586751.5:c.2550G>A
ENST00000587184.5:c.2777G>A	ENSP00000466557.1:p.Cys926Tyr
ENST00000588770.5:n.2350G>A
NM_000227.4:c.2945G>A	NP_000218.3:p.Cys982Tyr
NM_001127717.2:c.7604G>A	NP_001121189.2:p.Cys2535Tyr
NM_001127718.2:c.2777G>A	NP_001121190.2:p.Cys926Tyr
NM_198129.2:c.7772G>A	NP_937762.2:p.Cys2591Tyr
XM_011525978.1:c.7799G>A	XP_011524280.1:p.Cys2600Tyr
XM_011525979.1:c.7790G>A	XP_011524281.1:p.Cys2597Tyr
XM_011525980.1:c.7781G>A	XP_011524282.1:p.Cys2594Tyr
XM_011525981.1:c.7667G>A	XP_011524283.1:p.Cys2556Tyr
XM_011525982.1:c.7502G>A	XP_011524284.1:p.Cys2501Tyr
XM_011525978.2:c.7799G>A	XP_011524280.1:p.Cys2600Tyr
XM_011525979.2:c.7790G>A	XP_011524281.1:p.Cys2597Tyr
XM_011525980.2:c.7781G>A	XP_011524282.1:p.Cys2594Tyr
XM_011525981.2:c.7667G>A	XP_011524283.1:p.Cys2556Tyr
XM_011525982.2:c.7502G>A	XP_011524284.1:p.Cys2501Tyr
XM_017025743.1:c.5651G>A	XP_016881232.1:p.Cys1884Tyr
XM_017025744.1:c.3341G>A	XP_016881233.1:p.Cys1114Tyr
XR_001753199.1:n.8040G>A
NM_000227.5:c.2945G>A	NP_000218.3:p.Cys982Tyr
NM_001127717.3:c.7604G>A	NP_001121189.2:p.Cys2535Tyr
NM_001127718.3:c.2777G>A	NP_001121190.2:p.Cys926Tyr
NM_198129.3:c.7772G>A	NP_937762.2:p.Cys2591Tyr
NM_000227.6:c.2945G>A MANE Plus Clinical	NP_000218.3:p.Cys982Tyr
NM_001127717.4:c.7604G>A	NP_001121189.2:p.Cys2535Tyr
NM_001127718.4:c.2777G>A	NP_001121190.2:p.Cys926Tyr
NM_198129.4:c.7772G>A MANE Select	NP_937762.2:p.Cys2591Tyr