Canonical Allele Identifier: CA402063433

Gene: LAMA3

Linked Data

• COSMIC: COSM5792003 ; COSM5792004
• MyVariant Identifiers: chr18:g.21508195A>C (hg19) ; chr18:g.23928231A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928231A>C , CM000680.2:g.23928231A>C	GRCh38
NC_000018.9:g.21508195A>C , CM000680.1:g.21508195A>C	GRCh37
NC_000018.8:g.19762193A>C	NCBI36
NG_007853.2:g.243634A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3459A>C MANE Plus Clinical	ENSP00000269217.5:p.Glu1153Asp
ENST00000313654.14:c.8286A>C MANE Select	ENSP00000324532.8:p.Glu2762Asp
ENST00000649721.1:c.4881A>C	ENSP00000497885.1:p.Glu1627Asp
ENST00000269217.10:c.3459A>C	ENSP00000269217.5:p.Glu1153Asp
ENST00000313654.13:c.8286A>C	ENSP00000324532.8:p.Glu2762Asp
ENST00000399516.7:c.8118A>C	ENSP00000382432.2:p.Glu2706Asp
ENST00000586751.5:c.3064A>C
ENST00000587184.5:c.3291A>C	ENSP00000466557.1:p.Glu1097Asp
ENST00000588770.5:n.2864A>C
NM_000227.4:c.3459A>C	NP_000218.3:p.Glu1153Asp
NM_001127717.2:c.8118A>C	NP_001121189.2:p.Glu2706Asp
NM_001127718.2:c.3291A>C	NP_001121190.2:p.Glu1097Asp
NM_198129.2:c.8286A>C	NP_937762.2:p.Glu2762Asp
XM_011525978.1:c.8313A>C	XP_011524280.1:p.Glu2771Asp
XM_011525979.1:c.8304A>C	XP_011524281.1:p.Glu2768Asp
XM_011525980.1:c.8295A>C	XP_011524282.1:p.Glu2765Asp
XM_011525981.1:c.8181A>C	XP_011524283.1:p.Glu2727Asp
XM_011525982.1:c.8016A>C	XP_011524284.1:p.Glu2672Asp
XM_011525978.2:c.8313A>C	XP_011524280.1:p.Glu2771Asp
XM_011525979.2:c.8304A>C	XP_011524281.1:p.Glu2768Asp
XM_011525980.2:c.8295A>C	XP_011524282.1:p.Glu2765Asp
XM_011525981.2:c.8181A>C	XP_011524283.1:p.Glu2727Asp
XM_011525982.2:c.8016A>C	XP_011524284.1:p.Glu2672Asp
XM_017025743.1:c.6165A>C	XP_016881232.1:p.Glu2055Asp
XM_017025744.1:c.3855A>C	XP_016881233.1:p.Glu1285Asp
XR_001753199.1:n.8554A>C
NM_000227.5:c.3459A>C	NP_000218.3:p.Glu1153Asp
NM_001127717.3:c.8118A>C	NP_001121189.2:p.Glu2706Asp
NM_001127718.3:c.3291A>C	NP_001121190.2:p.Glu1097Asp
NM_198129.3:c.8286A>C	NP_937762.2:p.Glu2762Asp
NM_000227.6:c.3459A>C MANE Plus Clinical	NP_000218.3:p.Glu1153Asp
NM_001127717.4:c.8118A>C	NP_001121189.2:p.Glu2706Asp
NM_001127718.4:c.3291A>C	NP_001121190.2:p.Glu1097Asp
NM_198129.4:c.8286A>C MANE Select	NP_937762.2:p.Glu2762Asp