Canonical Allele Identifier: CA402051335

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21485516G>A (hg19) ; chr18:g.23905552G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23905552G>A , CM000680.2:g.23905552G>A	GRCh38
NC_000018.9:g.21485516G>A , CM000680.1:g.21485516G>A	GRCh37
NC_000018.8:g.19739514G>A	NCBI36
NG_007853.2:g.220955G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1819G>A MANE Plus Clinical	ENSP00000269217.5:p.Ala607Thr
ENST00000313654.14:c.6646G>A MANE Select	ENSP00000324532.8:p.Ala2216Thr
ENST00000649721.1:c.3538G>A	ENSP00000497885.1:p.Ala1180Thr
ENST00000269217.10:c.1819G>A	ENSP00000269217.5:p.Ala607Thr
ENST00000313654.13:c.6646G>A	ENSP00000324532.8:p.Ala2216Thr
ENST00000399516.7:c.6478G>A	ENSP00000382432.2:p.Ala2160Thr
ENST00000586751.5:c.1424G>A
ENST00000587184.5:c.1651G>A	ENSP00000466557.1:p.Ala551Thr
ENST00000588770.5:n.1224G>A
NM_000227.4:c.1819G>A	NP_000218.3:p.Ala607Thr
NM_001127717.2:c.6478G>A	NP_001121189.2:p.Ala2160Thr
NM_001127718.2:c.1651G>A	NP_001121190.2:p.Ala551Thr
NM_198129.2:c.6646G>A	NP_937762.2:p.Ala2216Thr
XM_011525978.1:c.6673G>A	XP_011524280.1:p.Ala2225Thr
XM_011525979.1:c.6664G>A	XP_011524281.1:p.Ala2222Thr
XM_011525980.1:c.6655G>A	XP_011524282.1:p.Ala2219Thr
XM_011525981.1:c.6541G>A	XP_011524283.1:p.Ala2181Thr
XM_011525982.1:c.6673G>A	XP_011524284.1:p.Ala2225Thr
XM_011525978.2:c.6673G>A	XP_011524280.1:p.Ala2225Thr
XM_011525979.2:c.6664G>A	XP_011524281.1:p.Ala2222Thr
XM_011525980.2:c.6655G>A	XP_011524282.1:p.Ala2219Thr
XM_011525981.2:c.6541G>A	XP_011524283.1:p.Ala2181Thr
XM_011525982.2:c.6673G>A	XP_011524284.1:p.Ala2225Thr
XM_017025743.1:c.4525G>A	XP_016881232.1:p.Ala1509Thr
XM_017025744.1:c.2215G>A	XP_016881233.1:p.Ala739Thr
XR_001753199.1:n.6914G>A
NM_000227.5:c.1819G>A	NP_000218.3:p.Ala607Thr
NM_001127717.3:c.6478G>A	NP_001121189.2:p.Ala2160Thr
NM_001127718.3:c.1651G>A	NP_001121190.2:p.Ala551Thr
NM_198129.3:c.6646G>A	NP_937762.2:p.Ala2216Thr
NM_000227.6:c.1819G>A MANE Plus Clinical	NP_000218.3:p.Ala607Thr
NM_001127717.4:c.6478G>A	NP_001121189.2:p.Ala2160Thr
NM_001127718.4:c.1651G>A	NP_001121190.2:p.Ala551Thr
NM_198129.4:c.6646G>A MANE Select	NP_937762.2:p.Ala2216Thr