Canonical Allele Identifier: CA503340637

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21508147T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928183T>A , CM000680.2:g.23928183T>A	GRCh38
NC_000018.9:g.21508147T>A , CM000680.1:g.21508147T>A	GRCh37
NC_000018.8:g.19762145T>A	NCBI36
NG_007853.2:g.243586T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3411T>A MANE Plus Clinical	ENSP00000269217.5:p.Gly1137=
ENST00000313654.14:c.8238T>A MANE Select	ENSP00000324532.8:p.Gly2746=
ENST00000649721.1:c.4833T>A	ENSP00000497885.1:p.Gly1611=
ENST00000269217.10:c.3411T>A	ENSP00000269217.5:p.Gly1137=
ENST00000313654.13:c.8238T>A	ENSP00000324532.8:p.Gly2746=
ENST00000399516.7:c.8070T>A	ENSP00000382432.2:p.Gly2690=
ENST00000586751.5:c.3016T>A
ENST00000587184.5:c.3243T>A	ENSP00000466557.1:p.Gly1081=
ENST00000588770.5:n.2816T>A
NM_000227.4:c.3411T>A	NP_000218.3:p.Gly1137=
NM_001127717.2:c.8070T>A	NP_001121189.2:p.Gly2690=
NM_001127718.2:c.3243T>A	NP_001121190.2:p.Gly1081=
NM_198129.2:c.8238T>A	NP_937762.2:p.Gly2746=
XM_011525978.1:c.8265T>A	XP_011524280.1:p.Gly2755=
XM_011525979.1:c.8256T>A	XP_011524281.1:p.Gly2752=
XM_011525980.1:c.8247T>A	XP_011524282.1:p.Gly2749=
XM_011525981.1:c.8133T>A	XP_011524283.1:p.Gly2711=
XM_011525982.1:c.7968T>A	XP_011524284.1:p.Gly2656=
XM_011525978.2:c.8265T>A	XP_011524280.1:p.Gly2755=
XM_011525979.2:c.8256T>A	XP_011524281.1:p.Gly2752=
XM_011525980.2:c.8247T>A	XP_011524282.1:p.Gly2749=
XM_011525981.2:c.8133T>A	XP_011524283.1:p.Gly2711=
XM_011525982.2:c.7968T>A	XP_011524284.1:p.Gly2656=
XM_017025743.1:c.6117T>A	XP_016881232.1:p.Gly2039=
XM_017025744.1:c.3807T>A	XP_016881233.1:p.Gly1269=
XR_001753199.1:n.8506T>A
NM_000227.5:c.3411T>A	NP_000218.3:p.Gly1137=
NM_001127717.3:c.8070T>A	NP_001121189.2:p.Gly2690=
NM_001127718.3:c.3243T>A	NP_001121190.2:p.Gly1081=
NM_198129.3:c.8238T>A	NP_937762.2:p.Gly2746=
NM_000227.6:c.3411T>A MANE Plus Clinical	NP_000218.3:p.Gly1137=
NM_001127717.4:c.8070T>A	NP_001121189.2:p.Gly2690=
NM_001127718.4:c.3243T>A	NP_001121190.2:p.Gly1081=
NM_198129.4:c.8238T>A MANE Select	NP_937762.2:p.Gly2746=