Canonical Allele Identifier: CA402064722

Gene: LAMA3

Linked Data

• COSMIC: COSM5015554 ; COSM5015555
• MyVariant Identifiers: chr18:g.21511093C>G (hg19) ; chr18:g.23931129C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23931129C>G , CM000680.2:g.23931129C>G	GRCh38
NC_000018.9:g.21511093C>G , CM000680.1:g.21511093C>G	GRCh37
NC_000018.8:g.19765091C>G	NCBI36
NG_007853.2:g.246532C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.3677C>G MANE Plus Clinical	ENSP00000269217.5:p.Pro1226Arg
ENST00000313654.14:c.8504C>G MANE Select	ENSP00000324532.8:p.Pro2835Arg
ENST00000649721.1:c.5099C>G	ENSP00000497885.1:p.Pro1700Arg
ENST00000269217.10:c.3677C>G	ENSP00000269217.5:p.Pro1226Arg
ENST00000313654.13:c.8504C>G	ENSP00000324532.8:p.Pro2835Arg
ENST00000399516.7:c.8336C>G	ENSP00000382432.2:p.Pro2779Arg
ENST00000586751.5:c.3282C>G
ENST00000587184.5:c.3509C>G	ENSP00000466557.1:p.Pro1170Arg
ENST00000588164.2:c.209C>G	ENSP00000467473.2:p.Pro70Arg
ENST00000588770.5:n.3082C>G
NM_000227.4:c.3677C>G	NP_000218.3:p.Pro1226Arg
NM_001127717.2:c.8336C>G	NP_001121189.2:p.Pro2779Arg
NM_001127718.2:c.3509C>G	NP_001121190.2:p.Pro1170Arg
NM_198129.2:c.8504C>G	NP_937762.2:p.Pro2835Arg
XM_011525978.1:c.8531C>G	XP_011524280.1:p.Pro2844Arg
XM_011525979.1:c.8522C>G	XP_011524281.1:p.Pro2841Arg
XM_011525980.1:c.8513C>G	XP_011524282.1:p.Pro2838Arg
XM_011525981.1:c.8399C>G	XP_011524283.1:p.Pro2800Arg
XM_011525982.1:c.8234C>G	XP_011524284.1:p.Pro2745Arg
XM_011525978.2:c.8531C>G	XP_011524280.1:p.Pro2844Arg
XM_011525979.2:c.8522C>G	XP_011524281.1:p.Pro2841Arg
XM_011525980.2:c.8513C>G	XP_011524282.1:p.Pro2838Arg
XM_011525981.2:c.8399C>G	XP_011524283.1:p.Pro2800Arg
XM_011525982.2:c.8234C>G	XP_011524284.1:p.Pro2745Arg
XM_017025743.1:c.6383C>G	XP_016881232.1:p.Pro2128Arg
XM_017025744.1:c.4073C>G	XP_016881233.1:p.Pro1358Arg
XR_001753199.1:n.8772C>G
NM_000227.5:c.3677C>G	NP_000218.3:p.Pro1226Arg
NM_001127717.3:c.8336C>G	NP_001121189.2:p.Pro2779Arg
NM_001127718.3:c.3509C>G	NP_001121190.2:p.Pro1170Arg
NM_198129.3:c.8504C>G	NP_937762.2:p.Pro2835Arg
NM_000227.6:c.3677C>G MANE Plus Clinical	NP_000218.3:p.Pro1226Arg
NM_001127717.4:c.8336C>G	NP_001121189.2:p.Pro2779Arg
NM_001127718.4:c.3509C>G	NP_001121190.2:p.Pro1170Arg
NM_198129.4:c.8504C>G MANE Select	NP_937762.2:p.Pro2835Arg