Canonical Allele Identifier: CA503339283

Gene: LAMA3

Linked Data

• COSMIC: COSM4071552 ; COSM4071553
• MyVariant Identifiers: chr18:g.21495282C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915318C>T , CM000680.2:g.23915318C>T	GRCh38
NC_000018.9:g.21495282C>T , CM000680.1:g.21495282C>T	GRCh37
NC_000018.8:g.19749280C>T	NCBI36
NG_007853.2:g.230721C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2847C>T MANE Plus Clinical	ENSP00000269217.5:p.Tyr949=
ENST00000313654.14:c.7674C>T MANE Select	ENSP00000324532.8:p.Tyr2558=
ENST00000649721.1:c.4269C>T	ENSP00000497885.1:p.Tyr1423=
ENST00000269217.10:c.2847C>T	ENSP00000269217.5:p.Tyr949=
ENST00000313654.13:c.7674C>T	ENSP00000324532.8:p.Tyr2558=
ENST00000399516.7:c.7506C>T	ENSP00000382432.2:p.Tyr2502=
ENST00000586751.5:c.2452C>T
ENST00000587184.5:c.2679C>T	ENSP00000466557.1:p.Tyr893=
ENST00000588770.5:n.2252C>T
NM_000227.4:c.2847C>T	NP_000218.3:p.Tyr949=
NM_001127717.2:c.7506C>T	NP_001121189.2:p.Tyr2502=
NM_001127718.2:c.2679C>T	NP_001121190.2:p.Tyr893=
NM_198129.2:c.7674C>T	NP_937762.2:p.Tyr2558=
XM_011525978.1:c.7701C>T	XP_011524280.1:p.Tyr2567=
XM_011525979.1:c.7692C>T	XP_011524281.1:p.Tyr2564=
XM_011525980.1:c.7683C>T	XP_011524282.1:p.Tyr2561=
XM_011525981.1:c.7569C>T	XP_011524283.1:p.Tyr2523=
XM_011525982.1:c.7404C>T	XP_011524284.1:p.Tyr2468=
XM_011525978.2:c.7701C>T	XP_011524280.1:p.Tyr2567=
XM_011525979.2:c.7692C>T	XP_011524281.1:p.Tyr2564=
XM_011525980.2:c.7683C>T	XP_011524282.1:p.Tyr2561=
XM_011525981.2:c.7569C>T	XP_011524283.1:p.Tyr2523=
XM_011525982.2:c.7404C>T	XP_011524284.1:p.Tyr2468=
XM_017025743.1:c.5553C>T	XP_016881232.1:p.Tyr1851=
XM_017025744.1:c.3243C>T	XP_016881233.1:p.Tyr1081=
XR_001753199.1:n.7942C>T
NM_000227.5:c.2847C>T	NP_000218.3:p.Tyr949=
NM_001127717.3:c.7506C>T	NP_001121189.2:p.Tyr2502=
NM_001127718.3:c.2679C>T	NP_001121190.2:p.Tyr893=
NM_198129.3:c.7674C>T	NP_937762.2:p.Tyr2558=
NM_000227.6:c.2847C>T MANE Plus Clinical	NP_000218.3:p.Tyr949=
NM_001127717.4:c.7506C>T	NP_001121189.2:p.Tyr2502=
NM_001127718.4:c.2679C>T	NP_001121190.2:p.Tyr893=
NM_198129.4:c.7674C>T MANE Select	NP_937762.2:p.Tyr2558=