Canonical Allele Identifier: CA402059382

Gene: LAMA3

Linked Data

• dbSNP Id: rs2081579401
• MyVariant Identifiers: chr18:g.21495382A>G (hg19) ; chr18:g.23915418A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915418A>G , CM000680.2:g.23915418A>G	GRCh38
NC_000018.9:g.21495382A>G , CM000680.1:g.21495382A>G	GRCh37
NC_000018.8:g.19749380A>G	NCBI36
NG_007853.2:g.230821A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2947A>G MANE Plus Clinical	ENSP00000269217.5:p.Arg983Gly
ENST00000313654.14:c.7774A>G MANE Select	ENSP00000324532.8:p.Arg2592Gly
ENST00000649721.1:c.4369A>G	ENSP00000497885.1:p.Arg1457Gly
ENST00000269217.10:c.2947A>G	ENSP00000269217.5:p.Arg983Gly
ENST00000313654.13:c.7774A>G	ENSP00000324532.8:p.Arg2592Gly
ENST00000399516.7:c.7606A>G	ENSP00000382432.2:p.Arg2536Gly
ENST00000586751.5:c.2552A>G
ENST00000587184.5:c.2779A>G	ENSP00000466557.1:p.Arg927Gly
ENST00000588770.5:n.2352A>G
NM_000227.4:c.2947A>G	NP_000218.3:p.Arg983Gly
NM_001127717.2:c.7606A>G	NP_001121189.2:p.Arg2536Gly
NM_001127718.2:c.2779A>G	NP_001121190.2:p.Arg927Gly
NM_198129.2:c.7774A>G	NP_937762.2:p.Arg2592Gly
XM_011525978.1:c.7801A>G	XP_011524280.1:p.Arg2601Gly
XM_011525979.1:c.7792A>G	XP_011524281.1:p.Arg2598Gly
XM_011525980.1:c.7783A>G	XP_011524282.1:p.Arg2595Gly
XM_011525981.1:c.7669A>G	XP_011524283.1:p.Arg2557Gly
XM_011525982.1:c.7504A>G	XP_011524284.1:p.Arg2502Gly
XM_011525978.2:c.7801A>G	XP_011524280.1:p.Arg2601Gly
XM_011525979.2:c.7792A>G	XP_011524281.1:p.Arg2598Gly
XM_011525980.2:c.7783A>G	XP_011524282.1:p.Arg2595Gly
XM_011525981.2:c.7669A>G	XP_011524283.1:p.Arg2557Gly
XM_011525982.2:c.7504A>G	XP_011524284.1:p.Arg2502Gly
XM_017025743.1:c.5653A>G	XP_016881232.1:p.Arg1885Gly
XM_017025744.1:c.3343A>G	XP_016881233.1:p.Arg1115Gly
XR_001753199.1:n.8042A>G
NM_000227.5:c.2947A>G	NP_000218.3:p.Arg983Gly
NM_001127717.3:c.7606A>G	NP_001121189.2:p.Arg2536Gly
NM_001127718.3:c.2779A>G	NP_001121190.2:p.Arg927Gly
NM_198129.3:c.7774A>G	NP_937762.2:p.Arg2592Gly
NM_000227.6:c.2947A>G MANE Plus Clinical	NP_000218.3:p.Arg983Gly
NM_001127717.4:c.7606A>G	NP_001121189.2:p.Arg2536Gly
NM_001127718.4:c.2779A>G	NP_001121190.2:p.Arg927Gly
NM_198129.4:c.7774A>G MANE Select	NP_937762.2:p.Arg2592Gly