Canonical Allele Identifier: CA402051821

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21529870G>A (hg19) ; chr18:g.23949906G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23949906G>A , CM000680.2:g.23949906G>A	GRCh38
NC_000018.9:g.21529870G>A , CM000680.1:g.21529870G>A	GRCh37
NC_000018.8:g.19783868G>A	NCBI36
NG_007853.2:g.265309G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.4666G>A MANE Plus Clinical	ENSP00000269217.5:p.Gly1556Arg
ENST00000313654.14:c.9493G>A MANE Select	ENSP00000324532.8:p.Gly3165Arg
ENST00000649721.1:c.6088G>A	ENSP00000497885.1:p.Gly2030Arg
ENST00000269217.10:c.4666G>A	ENSP00000269217.5:p.Gly1556Arg
ENST00000313654.13:c.9493G>A	ENSP00000324532.8:p.Gly3165Arg
ENST00000399516.7:c.9325G>A	ENSP00000382432.2:p.Gly3109Arg
ENST00000587184.5:c.4498G>A	ENSP00000466557.1:p.Gly1500Arg
ENST00000588004.1:c.14G>A
ENST00000588770.5:n.4071G>A
NM_000227.4:c.4666G>A	NP_000218.3:p.Gly1556Arg
NM_001127717.2:c.9325G>A	NP_001121189.2:p.Gly3109Arg
NM_001127718.2:c.4498G>A	NP_001121190.2:p.Gly1500Arg
NM_198129.2:c.9493G>A	NP_937762.2:p.Gly3165Arg
XM_011525978.1:c.9520G>A	XP_011524280.1:p.Gly3174Arg
XM_011525979.1:c.9511G>A	XP_011524281.1:p.Gly3171Arg
XM_011525980.1:c.9502G>A	XP_011524282.1:p.Gly3168Arg
XM_011525981.1:c.9388G>A	XP_011524283.1:p.Gly3130Arg
XM_011525982.1:c.9223G>A	XP_011524284.1:p.Gly3075Arg
XM_011525978.2:c.9520G>A	XP_011524280.1:p.Gly3174Arg
XM_011525979.2:c.9511G>A	XP_011524281.1:p.Gly3171Arg
XM_011525980.2:c.9502G>A	XP_011524282.1:p.Gly3168Arg
XM_011525981.2:c.9388G>A	XP_011524283.1:p.Gly3130Arg
XM_011525982.2:c.9223G>A	XP_011524284.1:p.Gly3075Arg
XM_017025743.1:c.7372G>A	XP_016881232.1:p.Gly2458Arg
XM_017025744.1:c.5062G>A	XP_016881233.1:p.Gly1688Arg
XR_001753199.1:n.9761G>A
NM_000227.5:c.4666G>A	NP_000218.3:p.Gly1556Arg
NM_001127717.3:c.9325G>A	NP_001121189.2:p.Gly3109Arg
NM_001127718.3:c.4498G>A	NP_001121190.2:p.Gly1500Arg
NM_198129.3:c.9493G>A	NP_937762.2:p.Gly3165Arg
NM_000227.6:c.4666G>A MANE Plus Clinical	NP_000218.3:p.Gly1556Arg
NM_001127717.4:c.9325G>A	NP_001121189.2:p.Gly3109Arg
NM_001127718.4:c.4498G>A	NP_001121190.2:p.Gly1500Arg
NM_198129.4:c.9493G>A MANE Select	NP_937762.2:p.Gly3165Arg