Canonical Allele Identifier: CA402044928

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21456295T>A (hg19) ; chr18:g.23876331T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23876331T>A , CM000680.2:g.23876331T>A	GRCh38
NC_000018.9:g.21456295T>A , CM000680.1:g.21456295T>A	GRCh37
NC_000018.8:g.19710293T>A	NCBI36
NG_007853.2:g.191734T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.209T>A MANE Plus Clinical	ENSP00000269217.5:p.Leu70Ter
ENST00000313654.14:c.5036T>A MANE Select	ENSP00000324532.8:p.Leu1679Ter
ENST00000649721.1:c.1928T>A	ENSP00000497885.1:p.Leu643Ter
ENST00000269217.10:c.209T>A	ENSP00000269217.5:p.Leu70Ter
ENST00000313654.13:c.5036T>A	ENSP00000324532.8:p.Leu1679Ter
ENST00000399516.7:c.5036T>A	ENSP00000382432.2:p.Leu1679Ter
ENST00000587184.5:c.209T>A	ENSP00000466557.1:p.Leu70Ter
NM_000227.4:c.209T>A	NP_000218.3:p.Leu70Ter
NM_001127717.2:c.5036T>A	NP_001121189.2:p.Leu1679Ter
NM_001127718.2:c.209T>A	NP_001121190.2:p.Leu70Ter
NM_198129.2:c.5036T>A	NP_937762.2:p.Leu1679Ter
XM_011525978.1:c.5063T>A	XP_011524280.1:p.Leu1688Ter
XM_011525979.1:c.5054T>A	XP_011524281.1:p.Leu1685Ter
XM_011525980.1:c.5045T>A	XP_011524282.1:p.Leu1682Ter
XM_011525981.1:c.4931T>A	XP_011524283.1:p.Leu1644Ter
XM_011525982.1:c.5063T>A	XP_011524284.1:p.Leu1688Ter
XM_011525978.2:c.5063T>A	XP_011524280.1:p.Leu1688Ter
XM_011525979.2:c.5054T>A	XP_011524281.1:p.Leu1685Ter
XM_011525980.2:c.5045T>A	XP_011524282.1:p.Leu1682Ter
XM_011525981.2:c.4931T>A	XP_011524283.1:p.Leu1644Ter
XM_011525982.2:c.5063T>A	XP_011524284.1:p.Leu1688Ter
XM_017025743.1:c.2915T>A	XP_016881232.1:p.Leu972Ter
XM_017025744.1:c.605T>A	XP_016881233.1:p.Leu202Ter
XR_001753199.1:n.5304T>A
NM_000227.5:c.209T>A	NP_000218.3:p.Leu70Ter
NM_001127717.3:c.5036T>A	NP_001121189.2:p.Leu1679Ter
NM_001127718.3:c.209T>A	NP_001121190.2:p.Leu70Ter
NM_198129.3:c.5036T>A	NP_937762.2:p.Leu1679Ter
NM_000227.6:c.209T>A MANE Plus Clinical	NP_000218.3:p.Leu70Ter
NM_001127717.4:c.5036T>A	NP_001121189.2:p.Leu1679Ter
NM_001127718.4:c.209T>A	NP_001121190.2:p.Leu70Ter
NM_198129.4:c.5036T>A MANE Select	NP_937762.2:p.Leu1679Ter