Canonical Allele Identifier: CA402059216

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21495322C>G (hg19) ; chr18:g.23915358C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915358C>G , CM000680.2:g.23915358C>G	GRCh38
NC_000018.9:g.21495322C>G , CM000680.1:g.21495322C>G	GRCh37
NC_000018.8:g.19749320C>G	NCBI36
NG_007853.2:g.230761C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2887C>G MANE Plus Clinical	ENSP00000269217.5:p.Leu963Val
ENST00000313654.14:c.7714C>G MANE Select	ENSP00000324532.8:p.Leu2572Val
ENST00000649721.1:c.4309C>G	ENSP00000497885.1:p.Leu1437Val
ENST00000269217.10:c.2887C>G	ENSP00000269217.5:p.Leu963Val
ENST00000313654.13:c.7714C>G	ENSP00000324532.8:p.Leu2572Val
ENST00000399516.7:c.7546C>G	ENSP00000382432.2:p.Leu2516Val
ENST00000586751.5:c.2492C>G
ENST00000587184.5:c.2719C>G	ENSP00000466557.1:p.Leu907Val
ENST00000588770.5:n.2292C>G
NM_000227.4:c.2887C>G	NP_000218.3:p.Leu963Val
NM_001127717.2:c.7546C>G	NP_001121189.2:p.Leu2516Val
NM_001127718.2:c.2719C>G	NP_001121190.2:p.Leu907Val
NM_198129.2:c.7714C>G	NP_937762.2:p.Leu2572Val
XM_011525978.1:c.7741C>G	XP_011524280.1:p.Leu2581Val
XM_011525979.1:c.7732C>G	XP_011524281.1:p.Leu2578Val
XM_011525980.1:c.7723C>G	XP_011524282.1:p.Leu2575Val
XM_011525981.1:c.7609C>G	XP_011524283.1:p.Leu2537Val
XM_011525982.1:c.7444C>G	XP_011524284.1:p.Leu2482Val
XM_011525978.2:c.7741C>G	XP_011524280.1:p.Leu2581Val
XM_011525979.2:c.7732C>G	XP_011524281.1:p.Leu2578Val
XM_011525980.2:c.7723C>G	XP_011524282.1:p.Leu2575Val
XM_011525981.2:c.7609C>G	XP_011524283.1:p.Leu2537Val
XM_011525982.2:c.7444C>G	XP_011524284.1:p.Leu2482Val
XM_017025743.1:c.5593C>G	XP_016881232.1:p.Leu1865Val
XM_017025744.1:c.3283C>G	XP_016881233.1:p.Leu1095Val
XR_001753199.1:n.7982C>G
NM_000227.5:c.2887C>G	NP_000218.3:p.Leu963Val
NM_001127717.3:c.7546C>G	NP_001121189.2:p.Leu2516Val
NM_001127718.3:c.2719C>G	NP_001121190.2:p.Leu907Val
NM_198129.3:c.7714C>G	NP_937762.2:p.Leu2572Val
NM_000227.6:c.2887C>G MANE Plus Clinical	NP_000218.3:p.Leu963Val
NM_001127717.4:c.7546C>G	NP_001121189.2:p.Leu2516Val
NM_001127718.4:c.2719C>G	NP_001121190.2:p.Leu907Val
NM_198129.4:c.7714C>G MANE Select	NP_937762.2:p.Leu2572Val