Canonical Allele Identifier: CA402044908

Gene: LAMA3

Linked Data

• dbSNP Id: rs779228347
• gnomAD v3: 18-23876322-A-G
• gnomAD v4: 18-23876322-A-G
• MyVariant Identifiers: chr18:g.21456286A>G (hg19) ; chr18:g.23876322A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23876322A>G , CM000680.2:g.23876322A>G	GRCh38
NC_000018.9:g.21456286A>G , CM000680.1:g.21456286A>G	GRCh37
NC_000018.8:g.19710284A>G	NCBI36
NG_007853.2:g.191725A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.200A>G MANE Plus Clinical	ENSP00000269217.5:p.His67Arg
ENST00000313654.14:c.5027A>G MANE Select	ENSP00000324532.8:p.His1676Arg
ENST00000649721.1:c.1919A>G	ENSP00000497885.1:p.His640Arg
ENST00000269217.10:c.200A>G	ENSP00000269217.5:p.His67Arg
ENST00000313654.13:c.5027A>G	ENSP00000324532.8:p.His1676Arg
ENST00000399516.7:c.5027A>G	ENSP00000382432.2:p.His1676Arg
ENST00000587184.5:c.200A>G	ENSP00000466557.1:p.His67Arg
NM_000227.4:c.200A>G	NP_000218.3:p.His67Arg
NM_001127717.2:c.5027A>G	NP_001121189.2:p.His1676Arg
NM_001127718.2:c.200A>G	NP_001121190.2:p.His67Arg
NM_198129.2:c.5027A>G	NP_937762.2:p.His1676Arg
XM_011525978.1:c.5054A>G	XP_011524280.1:p.His1685Arg
XM_011525979.1:c.5045A>G	XP_011524281.1:p.His1682Arg
XM_011525980.1:c.5036A>G	XP_011524282.1:p.His1679Arg
XM_011525981.1:c.4922A>G	XP_011524283.1:p.His1641Arg
XM_011525982.1:c.5054A>G	XP_011524284.1:p.His1685Arg
XM_011525978.2:c.5054A>G	XP_011524280.1:p.His1685Arg
XM_011525979.2:c.5045A>G	XP_011524281.1:p.His1682Arg
XM_011525980.2:c.5036A>G	XP_011524282.1:p.His1679Arg
XM_011525981.2:c.4922A>G	XP_011524283.1:p.His1641Arg
XM_011525982.2:c.5054A>G	XP_011524284.1:p.His1685Arg
XM_017025743.1:c.2906A>G	XP_016881232.1:p.His969Arg
XM_017025744.1:c.596A>G	XP_016881233.1:p.His199Arg
XR_001753199.1:n.5295A>G
NM_000227.5:c.200A>G	NP_000218.3:p.His67Arg
NM_001127717.3:c.5027A>G	NP_001121189.2:p.His1676Arg
NM_001127718.3:c.200A>G	NP_001121190.2:p.His67Arg
NM_198129.3:c.5027A>G	NP_937762.2:p.His1676Arg
NM_000227.6:c.200A>G MANE Plus Clinical	NP_000218.3:p.His67Arg
NM_001127717.4:c.5027A>G	NP_001121189.2:p.His1676Arg
NM_001127718.4:c.200A>G	NP_001121190.2:p.His67Arg
NM_198129.4:c.5027A>G MANE Select	NP_937762.2:p.His1676Arg