Canonical Allele Identifier: CA402048716

Gene: LAMA3

Linked Data

• dbSNP Id: rs2081126609
• gnomAD v3: 18-23903039-A-G
• gnomAD v4: 18-23903039-A-G
• COSMIC: COSM4140025 ; COSM4140026
• MyVariant Identifiers: chr18:g.21483003A>G (hg19) ; chr18:g.23903039A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23903039A>G , CM000680.2:g.23903039A>G	GRCh38
NC_000018.9:g.21483003A>G , CM000680.1:g.21483003A>G	GRCh37
NC_000018.8:g.19737001A>G	NCBI36
NG_007853.2:g.218442A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1405A>G MANE Plus Clinical	ENSP00000269217.5:p.Ser469Gly
ENST00000313654.14:c.6232A>G MANE Select	ENSP00000324532.8:p.Ser2078Gly
ENST00000649721.1:c.3124A>G	ENSP00000497885.1:p.Ser1042Gly
ENST00000269217.10:c.1405A>G	ENSP00000269217.5:p.Ser469Gly
ENST00000313654.13:c.6232A>G	ENSP00000324532.8:p.Ser2078Gly
ENST00000399516.7:c.6064A>G	ENSP00000382432.2:p.Ser2022Gly
ENST00000586751.5:c.1010A>G
ENST00000587184.5:c.1237A>G	ENSP00000466557.1:p.Ser413Gly
ENST00000588770.5:n.810A>G
NM_000227.4:c.1405A>G	NP_000218.3:p.Ser469Gly
NM_001127717.2:c.6064A>G	NP_001121189.2:p.Ser2022Gly
NM_001127718.2:c.1237A>G	NP_001121190.2:p.Ser413Gly
NM_198129.2:c.6232A>G	NP_937762.2:p.Ser2078Gly
XM_011525978.1:c.6259A>G	XP_011524280.1:p.Ser2087Gly
XM_011525979.1:c.6250A>G	XP_011524281.1:p.Ser2084Gly
XM_011525980.1:c.6241A>G	XP_011524282.1:p.Ser2081Gly
XM_011525981.1:c.6127A>G	XP_011524283.1:p.Ser2043Gly
XM_011525982.1:c.6259A>G	XP_011524284.1:p.Ser2087Gly
XM_011525978.2:c.6259A>G	XP_011524280.1:p.Ser2087Gly
XM_011525979.2:c.6250A>G	XP_011524281.1:p.Ser2084Gly
XM_011525980.2:c.6241A>G	XP_011524282.1:p.Ser2081Gly
XM_011525981.2:c.6127A>G	XP_011524283.1:p.Ser2043Gly
XM_011525982.2:c.6259A>G	XP_011524284.1:p.Ser2087Gly
XM_017025743.1:c.4111A>G	XP_016881232.1:p.Ser1371Gly
XM_017025744.1:c.1801A>G	XP_016881233.1:p.Ser601Gly
XR_001753199.1:n.6500A>G
NM_000227.5:c.1405A>G	NP_000218.3:p.Ser469Gly
NM_001127717.3:c.6064A>G	NP_001121189.2:p.Ser2022Gly
NM_001127718.3:c.1237A>G	NP_001121190.2:p.Ser413Gly
NM_198129.3:c.6232A>G	NP_937762.2:p.Ser2078Gly
NM_000227.6:c.1405A>G MANE Plus Clinical	NP_000218.3:p.Ser469Gly
NM_001127717.4:c.6064A>G	NP_001121189.2:p.Ser2022Gly
NM_001127718.4:c.1237A>G	NP_001121190.2:p.Ser413Gly
NM_198129.4:c.6232A>G MANE Select	NP_937762.2:p.Ser2078Gly