Canonical Allele Identifier: CA402059386

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21495384A>C (hg19) ; chr18:g.23915420A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915420A>C , CM000680.2:g.23915420A>C	GRCh38
NC_000018.9:g.21495384A>C , CM000680.1:g.21495384A>C	GRCh37
NC_000018.8:g.19749382A>C	NCBI36
NG_007853.2:g.230823A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2949A>C MANE Plus Clinical	ENSP00000269217.5:p.Arg983Ser
ENST00000313654.14:c.7776A>C MANE Select	ENSP00000324532.8:p.Arg2592Ser
ENST00000649721.1:c.4371A>C	ENSP00000497885.1:p.Arg1457Ser
ENST00000269217.10:c.2949A>C	ENSP00000269217.5:p.Arg983Ser
ENST00000313654.13:c.7776A>C	ENSP00000324532.8:p.Arg2592Ser
ENST00000399516.7:c.7608A>C	ENSP00000382432.2:p.Arg2536Ser
ENST00000586751.5:c.2554A>C
ENST00000587184.5:c.2781A>C	ENSP00000466557.1:p.Arg927Ser
ENST00000588770.5:n.2354A>C
NM_000227.4:c.2949A>C	NP_000218.3:p.Arg983Ser
NM_001127717.2:c.7608A>C	NP_001121189.2:p.Arg2536Ser
NM_001127718.2:c.2781A>C	NP_001121190.2:p.Arg927Ser
NM_198129.2:c.7776A>C	NP_937762.2:p.Arg2592Ser
XM_011525978.1:c.7803A>C	XP_011524280.1:p.Arg2601Ser
XM_011525979.1:c.7794A>C	XP_011524281.1:p.Arg2598Ser
XM_011525980.1:c.7785A>C	XP_011524282.1:p.Arg2595Ser
XM_011525981.1:c.7671A>C	XP_011524283.1:p.Arg2557Ser
XM_011525982.1:c.7506A>C	XP_011524284.1:p.Arg2502Ser
XM_011525978.2:c.7803A>C	XP_011524280.1:p.Arg2601Ser
XM_011525979.2:c.7794A>C	XP_011524281.1:p.Arg2598Ser
XM_011525980.2:c.7785A>C	XP_011524282.1:p.Arg2595Ser
XM_011525981.2:c.7671A>C	XP_011524283.1:p.Arg2557Ser
XM_011525982.2:c.7506A>C	XP_011524284.1:p.Arg2502Ser
XM_017025743.1:c.5655A>C	XP_016881232.1:p.Arg1885Ser
XM_017025744.1:c.3345A>C	XP_016881233.1:p.Arg1115Ser
XR_001753199.1:n.8044A>C
NM_000227.5:c.2949A>C	NP_000218.3:p.Arg983Ser
NM_001127717.3:c.7608A>C	NP_001121189.2:p.Arg2536Ser
NM_001127718.3:c.2781A>C	NP_001121190.2:p.Arg927Ser
NM_198129.3:c.7776A>C	NP_937762.2:p.Arg2592Ser
NM_000227.6:c.2949A>C MANE Plus Clinical	NP_000218.3:p.Arg983Ser
NM_001127717.4:c.7608A>C	NP_001121189.2:p.Arg2536Ser
NM_001127718.4:c.2781A>C	NP_001121190.2:p.Arg927Ser
NM_198129.4:c.7776A>C MANE Select	NP_937762.2:p.Arg2592Ser