Canonical Allele Identifier: CA402063035

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21508122T>A (hg19) ; chr18:g.23928158T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928158T>A , CM000680.2:g.23928158T>A	GRCh38
NC_000018.9:g.21508122T>A , CM000680.1:g.21508122T>A	GRCh37
NC_000018.8:g.19762120T>A	NCBI36
NG_007853.2:g.243561T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.3386T>A MANE Plus Clinical	ENSP00000269217.5:p.Met1129Lys
ENST00000313654.14:c.8213T>A MANE Select	ENSP00000324532.8:p.Met2738Lys
ENST00000649721.1:c.4808T>A	ENSP00000497885.1:p.Met1603Lys
ENST00000269217.10:c.3386T>A	ENSP00000269217.5:p.Met1129Lys
ENST00000313654.13:c.8213T>A	ENSP00000324532.8:p.Met2738Lys
ENST00000399516.7:c.8045T>A	ENSP00000382432.2:p.Met2682Lys
ENST00000586751.5:c.2991T>A
ENST00000587184.5:c.3218T>A	ENSP00000466557.1:p.Met1073Lys
ENST00000588770.5:n.2791T>A
NM_000227.4:c.3386T>A	NP_000218.3:p.Met1129Lys
NM_001127717.2:c.8045T>A	NP_001121189.2:p.Met2682Lys
NM_001127718.2:c.3218T>A	NP_001121190.2:p.Met1073Lys
NM_198129.2:c.8213T>A	NP_937762.2:p.Met2738Lys
XM_011525978.1:c.8240T>A	XP_011524280.1:p.Met2747Lys
XM_011525979.1:c.8231T>A	XP_011524281.1:p.Met2744Lys
XM_011525980.1:c.8222T>A	XP_011524282.1:p.Met2741Lys
XM_011525981.1:c.8108T>A	XP_011524283.1:p.Met2703Lys
XM_011525982.1:c.7943T>A	XP_011524284.1:p.Met2648Lys
XM_011525978.2:c.8240T>A	XP_011524280.1:p.Met2747Lys
XM_011525979.2:c.8231T>A	XP_011524281.1:p.Met2744Lys
XM_011525980.2:c.8222T>A	XP_011524282.1:p.Met2741Lys
XM_011525981.2:c.8108T>A	XP_011524283.1:p.Met2703Lys
XM_011525982.2:c.7943T>A	XP_011524284.1:p.Met2648Lys
XM_017025743.1:c.6092T>A	XP_016881232.1:p.Met2031Lys
XM_017025744.1:c.3782T>A	XP_016881233.1:p.Met1261Lys
XR_001753199.1:n.8481T>A
NM_000227.5:c.3386T>A	NP_000218.3:p.Met1129Lys
NM_001127717.3:c.8045T>A	NP_001121189.2:p.Met2682Lys
NM_001127718.3:c.3218T>A	NP_001121190.2:p.Met1073Lys
NM_198129.3:c.8213T>A	NP_937762.2:p.Met2738Lys
NM_000227.6:c.3386T>A MANE Plus Clinical	NP_000218.3:p.Met1129Lys
NM_001127717.4:c.8045T>A	NP_001121189.2:p.Met2682Lys
NM_001127718.4:c.3218T>A	NP_001121190.2:p.Met1073Lys
NM_198129.4:c.8213T>A MANE Select	NP_937762.2:p.Met2738Lys