Canonical Allele Identifier: CA402048729

Gene: LAMA3

Linked Data

• dbSNP Id: rs2081126838
• MyVariant Identifiers: chr18:g.21483006G>A (hg19) ; chr18:g.23903042G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23903042G>A , CM000680.2:g.23903042G>A	GRCh38
NC_000018.9:g.21483006G>A , CM000680.1:g.21483006G>A	GRCh37
NC_000018.8:g.19737004G>A	NCBI36
NG_007853.2:g.218445G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1408G>A MANE Plus Clinical	ENSP00000269217.5:p.Asp470Asn
ENST00000313654.14:c.6235G>A MANE Select	ENSP00000324532.8:p.Asp2079Asn
ENST00000649721.1:c.3127G>A	ENSP00000497885.1:p.Asp1043Asn
ENST00000269217.10:c.1408G>A	ENSP00000269217.5:p.Asp470Asn
ENST00000313654.13:c.6235G>A	ENSP00000324532.8:p.Asp2079Asn
ENST00000399516.7:c.6067G>A	ENSP00000382432.2:p.Asp2023Asn
ENST00000586751.5:c.1013G>A
ENST00000587184.5:c.1240G>A	ENSP00000466557.1:p.Asp414Asn
ENST00000588770.5:n.813G>A
NM_000227.4:c.1408G>A	NP_000218.3:p.Asp470Asn
NM_001127717.2:c.6067G>A	NP_001121189.2:p.Asp2023Asn
NM_001127718.2:c.1240G>A	NP_001121190.2:p.Asp414Asn
NM_198129.2:c.6235G>A	NP_937762.2:p.Asp2079Asn
XM_011525978.1:c.6262G>A	XP_011524280.1:p.Asp2088Asn
XM_011525979.1:c.6253G>A	XP_011524281.1:p.Asp2085Asn
XM_011525980.1:c.6244G>A	XP_011524282.1:p.Asp2082Asn
XM_011525981.1:c.6130G>A	XP_011524283.1:p.Asp2044Asn
XM_011525982.1:c.6262G>A	XP_011524284.1:p.Asp2088Asn
XM_011525978.2:c.6262G>A	XP_011524280.1:p.Asp2088Asn
XM_011525979.2:c.6253G>A	XP_011524281.1:p.Asp2085Asn
XM_011525980.2:c.6244G>A	XP_011524282.1:p.Asp2082Asn
XM_011525981.2:c.6130G>A	XP_011524283.1:p.Asp2044Asn
XM_011525982.2:c.6262G>A	XP_011524284.1:p.Asp2088Asn
XM_017025743.1:c.4114G>A	XP_016881232.1:p.Asp1372Asn
XM_017025744.1:c.1804G>A	XP_016881233.1:p.Asp602Asn
XR_001753199.1:n.6503G>A
NM_000227.5:c.1408G>A	NP_000218.3:p.Asp470Asn
NM_001127717.3:c.6067G>A	NP_001121189.2:p.Asp2023Asn
NM_001127718.3:c.1240G>A	NP_001121190.2:p.Asp414Asn
NM_198129.3:c.6235G>A	NP_937762.2:p.Asp2079Asn
NM_000227.6:c.1408G>A MANE Plus Clinical	NP_000218.3:p.Asp470Asn
NM_001127717.4:c.6067G>A	NP_001121189.2:p.Asp2023Asn
NM_001127718.4:c.1240G>A	NP_001121190.2:p.Asp414Asn
NM_198129.4:c.6235G>A MANE Select	NP_937762.2:p.Asp2079Asn