Canonical Allele Identifier: CA402051305

Gene: LAMA3

Linked Data

• gnomAD v4: 18-23905540-C-A
• MyVariant Identifiers: chr18:g.21485504C>A (hg19) ; chr18:g.23905540C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23905540C>A , CM000680.2:g.23905540C>A	GRCh38
NC_000018.9:g.21485504C>A , CM000680.1:g.21485504C>A	GRCh37
NC_000018.8:g.19739502C>A	NCBI36
NG_007853.2:g.220943C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1807C>A MANE Plus Clinical	ENSP00000269217.5:p.Leu603Met
ENST00000313654.14:c.6634C>A MANE Select	ENSP00000324532.8:p.Leu2212Met
ENST00000649721.1:c.3526C>A	ENSP00000497885.1:p.Leu1176Met
ENST00000269217.10:c.1807C>A	ENSP00000269217.5:p.Leu603Met
ENST00000313654.13:c.6634C>A	ENSP00000324532.8:p.Leu2212Met
ENST00000399516.7:c.6466C>A	ENSP00000382432.2:p.Leu2156Met
ENST00000586751.5:c.1412C>A
ENST00000587184.5:c.1639C>A	ENSP00000466557.1:p.Leu547Met
ENST00000588770.5:n.1212C>A
NM_000227.4:c.1807C>A	NP_000218.3:p.Leu603Met
NM_001127717.2:c.6466C>A	NP_001121189.2:p.Leu2156Met
NM_001127718.2:c.1639C>A	NP_001121190.2:p.Leu547Met
NM_198129.2:c.6634C>A	NP_937762.2:p.Leu2212Met
XM_011525978.1:c.6661C>A	XP_011524280.1:p.Leu2221Met
XM_011525979.1:c.6652C>A	XP_011524281.1:p.Leu2218Met
XM_011525980.1:c.6643C>A	XP_011524282.1:p.Leu2215Met
XM_011525981.1:c.6529C>A	XP_011524283.1:p.Leu2177Met
XM_011525982.1:c.6661C>A	XP_011524284.1:p.Leu2221Met
XM_011525978.2:c.6661C>A	XP_011524280.1:p.Leu2221Met
XM_011525979.2:c.6652C>A	XP_011524281.1:p.Leu2218Met
XM_011525980.2:c.6643C>A	XP_011524282.1:p.Leu2215Met
XM_011525981.2:c.6529C>A	XP_011524283.1:p.Leu2177Met
XM_011525982.2:c.6661C>A	XP_011524284.1:p.Leu2221Met
XM_017025743.1:c.4513C>A	XP_016881232.1:p.Leu1505Met
XM_017025744.1:c.2203C>A	XP_016881233.1:p.Leu735Met
XR_001753199.1:n.6902C>A
NM_000227.5:c.1807C>A	NP_000218.3:p.Leu603Met
NM_001127717.3:c.6466C>A	NP_001121189.2:p.Leu2156Met
NM_001127718.3:c.1639C>A	NP_001121190.2:p.Leu547Met
NM_198129.3:c.6634C>A	NP_937762.2:p.Leu2212Met
NM_000227.6:c.1807C>A MANE Plus Clinical	NP_000218.3:p.Leu603Met
NM_001127717.4:c.6466C>A	NP_001121189.2:p.Leu2156Met
NM_001127718.4:c.1639C>A	NP_001121190.2:p.Leu547Met
NM_198129.4:c.6634C>A MANE Select	NP_937762.2:p.Leu2212Met