Canonical Allele Identifier: CA503335021

Gene: LAMA3

Linked Data

• gnomAD v4: 18-23903125-G-A
• MyVariant Identifiers: chr18:g.21483089G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23903125G>A , CM000680.2:g.23903125G>A	GRCh38
NC_000018.9:g.21483089G>A , CM000680.1:g.21483089G>A	GRCh37
NC_000018.8:g.19737087G>A	NCBI36
NG_007853.2:g.218528G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1491G>A MANE Plus Clinical	ENSP00000269217.5:p.Lys497=
ENST00000313654.14:c.6318G>A MANE Select	ENSP00000324532.8:p.Lys2106=
ENST00000649721.1:c.3210G>A	ENSP00000497885.1:p.Lys1070=
ENST00000269217.10:c.1491G>A	ENSP00000269217.5:p.Lys497=
ENST00000313654.13:c.6318G>A	ENSP00000324532.8:p.Lys2106=
ENST00000399516.7:c.6150G>A	ENSP00000382432.2:p.Lys2050=
ENST00000586751.5:c.1096G>A
ENST00000587184.5:c.1323G>A	ENSP00000466557.1:p.Lys441=
ENST00000588770.5:n.896G>A
NM_000227.4:c.1491G>A	NP_000218.3:p.Lys497=
NM_001127717.2:c.6150G>A	NP_001121189.2:p.Lys2050=
NM_001127718.2:c.1323G>A	NP_001121190.2:p.Lys441=
NM_198129.2:c.6318G>A	NP_937762.2:p.Lys2106=
XM_011525978.1:c.6345G>A	XP_011524280.1:p.Lys2115=
XM_011525979.1:c.6336G>A	XP_011524281.1:p.Lys2112=
XM_011525980.1:c.6327G>A	XP_011524282.1:p.Lys2109=
XM_011525981.1:c.6213G>A	XP_011524283.1:p.Lys2071=
XM_011525982.1:c.6345G>A	XP_011524284.1:p.Lys2115=
XM_011525978.2:c.6345G>A	XP_011524280.1:p.Lys2115=
XM_011525979.2:c.6336G>A	XP_011524281.1:p.Lys2112=
XM_011525980.2:c.6327G>A	XP_011524282.1:p.Lys2109=
XM_011525981.2:c.6213G>A	XP_011524283.1:p.Lys2071=
XM_011525982.2:c.6345G>A	XP_011524284.1:p.Lys2115=
XM_017025743.1:c.4197G>A	XP_016881232.1:p.Lys1399=
XM_017025744.1:c.1887G>A	XP_016881233.1:p.Lys629=
XR_001753199.1:n.6586G>A
NM_000227.5:c.1491G>A	NP_000218.3:p.Lys497=
NM_001127717.3:c.6150G>A	NP_001121189.2:p.Lys2050=
NM_001127718.3:c.1323G>A	NP_001121190.2:p.Lys441=
NM_198129.3:c.6318G>A	NP_937762.2:p.Lys2106=
NM_000227.6:c.1491G>A MANE Plus Clinical	NP_000218.3:p.Lys497=
NM_001127717.4:c.6150G>A	NP_001121189.2:p.Lys2050=
NM_001127718.4:c.1323G>A	NP_001121190.2:p.Lys441=
NM_198129.4:c.6318G>A MANE Select	NP_937762.2:p.Lys2106=