Canonical Allele Identifier: CA503336580

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21485518T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23905554T>G , CM000680.2:g.23905554T>G	GRCh38
NC_000018.9:g.21485518T>G , CM000680.1:g.21485518T>G	GRCh37
NC_000018.8:g.19739516T>G	NCBI36
NG_007853.2:g.220957T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1821T>G MANE Plus Clinical	ENSP00000269217.5:p.Ala607=
ENST00000313654.14:c.6648T>G MANE Select	ENSP00000324532.8:p.Ala2216=
ENST00000649721.1:c.3540T>G	ENSP00000497885.1:p.Ala1180=
ENST00000269217.10:c.1821T>G	ENSP00000269217.5:p.Ala607=
ENST00000313654.13:c.6648T>G	ENSP00000324532.8:p.Ala2216=
ENST00000399516.7:c.6480T>G	ENSP00000382432.2:p.Ala2160=
ENST00000586751.5:c.1426T>G
ENST00000587184.5:c.1653T>G	ENSP00000466557.1:p.Ala551=
ENST00000588770.5:n.1226T>G
NM_000227.4:c.1821T>G	NP_000218.3:p.Ala607=
NM_001127717.2:c.6480T>G	NP_001121189.2:p.Ala2160=
NM_001127718.2:c.1653T>G	NP_001121190.2:p.Ala551=
NM_198129.2:c.6648T>G	NP_937762.2:p.Ala2216=
XM_011525978.1:c.6675T>G	XP_011524280.1:p.Ala2225=
XM_011525979.1:c.6666T>G	XP_011524281.1:p.Ala2222=
XM_011525980.1:c.6657T>G	XP_011524282.1:p.Ala2219=
XM_011525981.1:c.6543T>G	XP_011524283.1:p.Ala2181=
XM_011525982.1:c.6675T>G	XP_011524284.1:p.Ala2225=
XM_011525978.2:c.6675T>G	XP_011524280.1:p.Ala2225=
XM_011525979.2:c.6666T>G	XP_011524281.1:p.Ala2222=
XM_011525980.2:c.6657T>G	XP_011524282.1:p.Ala2219=
XM_011525981.2:c.6543T>G	XP_011524283.1:p.Ala2181=
XM_011525982.2:c.6675T>G	XP_011524284.1:p.Ala2225=
XM_017025743.1:c.4527T>G	XP_016881232.1:p.Ala1509=
XM_017025744.1:c.2217T>G	XP_016881233.1:p.Ala739=
XR_001753199.1:n.6916T>G
NM_000227.5:c.1821T>G	NP_000218.3:p.Ala607=
NM_001127717.3:c.6480T>G	NP_001121189.2:p.Ala2160=
NM_001127718.3:c.1653T>G	NP_001121190.2:p.Ala551=
NM_198129.3:c.6648T>G	NP_937762.2:p.Ala2216=
NM_000227.6:c.1821T>G MANE Plus Clinical	NP_000218.3:p.Ala607=
NM_001127717.4:c.6480T>G	NP_001121189.2:p.Ala2160=
NM_001127718.4:c.1653T>G	NP_001121190.2:p.Ala551=
NM_198129.4:c.6648T>G MANE Select	NP_937762.2:p.Ala2216=