Canonical Allele Identifier: CA2840937934

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23905558dup , CM000680.2:g.23905558dup	GRCh38
NC_000018.9:g.21485522dup , CM000680.1:g.21485522dup	GRCh37
NC_000018.8:g.19739520dup	NCBI36
NG_007853.2:g.220961dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1825dup MANE Plus Clinical	ENSP00000269217.5:p.Thr609AsnfsTer7
ENST00000313654.14:c.6652dup MANE Select	ENSP00000324532.8:p.Thr2218AsnfsTer7
ENST00000649721.1:c.3544dup	ENSP00000497885.1:p.Thr1182AsnfsTer7
ENST00000269217.10:c.1825dup	ENSP00000269217.5:p.Thr609AsnfsTer7
ENST00000313654.13:c.6652dup	ENSP00000324532.8:p.Thr2218AsnfsTer7
ENST00000399516.7:c.6484dup	ENSP00000382432.2:p.Thr2162AsnfsTer7
ENST00000586751.5:c.1430dup
ENST00000587184.5:c.1657dup	ENSP00000466557.1:p.Thr553AsnfsTer7
ENST00000588770.5:n.1230dup
NM_000227.4:c.1825dup	NP_000218.3:p.Thr609AsnfsTer7
NM_001127717.2:c.6484dup	NP_001121189.2:p.Thr2162AsnfsTer7
NM_001127718.2:c.1657dup	NP_001121190.2:p.Thr553AsnfsTer7
NM_198129.2:c.6652dup	NP_937762.2:p.Thr2218AsnfsTer7
XM_011525978.1:c.6679dup	XP_011524280.1:p.Thr2227AsnfsTer7
XM_011525979.1:c.6670dup	XP_011524281.1:p.Thr2224AsnfsTer7
XM_011525980.1:c.6661dup	XP_011524282.1:p.Thr2221AsnfsTer7
XM_011525981.1:c.6547dup	XP_011524283.1:p.Thr2183AsnfsTer7
XM_011525982.1:c.6679dup	XP_011524284.1:p.Thr2227AsnfsTer7
XM_011525978.2:c.6679dup	XP_011524280.1:p.Thr2227AsnfsTer7
XM_011525979.2:c.6670dup	XP_011524281.1:p.Thr2224AsnfsTer7
XM_011525980.2:c.6661dup	XP_011524282.1:p.Thr2221AsnfsTer7
XM_011525981.2:c.6547dup	XP_011524283.1:p.Thr2183AsnfsTer7
XM_011525982.2:c.6679dup	XP_011524284.1:p.Thr2227AsnfsTer7
XM_017025743.1:c.4531dup	XP_016881232.1:p.Thr1511AsnfsTer7
XM_017025744.1:c.2221dup	XP_016881233.1:p.Thr741AsnfsTer7
XR_001753199.1:n.6920dup
NM_000227.5:c.1825dup	NP_000218.3:p.Thr609AsnfsTer7
NM_001127717.3:c.6484dup	NP_001121189.2:p.Thr2162AsnfsTer7
NM_001127718.3:c.1657dup	NP_001121190.2:p.Thr553AsnfsTer7
NM_198129.3:c.6652dup	NP_937762.2:p.Thr2218AsnfsTer7
NM_000227.6:c.1825dup MANE Plus Clinical	NP_000218.3:p.Thr609AsnfsTer7
NM_001127717.4:c.6484dup	NP_001121189.2:p.Thr2162AsnfsTer7
NM_001127718.4:c.1657dup	NP_001121190.2:p.Thr553AsnfsTer7
NM_198129.4:c.6652dup MANE Select	NP_937762.2:p.Thr2218AsnfsTer7