Canonical Allele Identifier: CA402064707

Gene: LAMA3

Linked Data

• dbSNP Id: rs1426717095
• gnomAD v2: 18-21511090-G-A
• gnomAD v4: 18-23931126-G-A
• MyVariant Identifiers: chr18:g.21511090G>A (hg19) ; chr18:g.23931126G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23931126G>A , CM000680.2:g.23931126G>A	GRCh38
NC_000018.9:g.21511090G>A , CM000680.1:g.21511090G>A	GRCh37
NC_000018.8:g.19765088G>A	NCBI36
NG_007853.2:g.246529G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.3674G>A MANE Plus Clinical	ENSP00000269217.5:p.Gly1225Asp
ENST00000313654.14:c.8501G>A MANE Select	ENSP00000324532.8:p.Gly2834Asp
ENST00000649721.1:c.5096G>A	ENSP00000497885.1:p.Gly1699Asp
ENST00000269217.10:c.3674G>A	ENSP00000269217.5:p.Gly1225Asp
ENST00000313654.13:c.8501G>A	ENSP00000324532.8:p.Gly2834Asp
ENST00000399516.7:c.8333G>A	ENSP00000382432.2:p.Gly2778Asp
ENST00000586751.5:c.3279G>A
ENST00000587184.5:c.3506G>A	ENSP00000466557.1:p.Gly1169Asp
ENST00000588164.2:c.206G>A	ENSP00000467473.2:p.Gly69Asp
ENST00000588770.5:n.3079G>A
NM_000227.4:c.3674G>A	NP_000218.3:p.Gly1225Asp
NM_001127717.2:c.8333G>A	NP_001121189.2:p.Gly2778Asp
NM_001127718.2:c.3506G>A	NP_001121190.2:p.Gly1169Asp
NM_198129.2:c.8501G>A	NP_937762.2:p.Gly2834Asp
XM_011525978.1:c.8528G>A	XP_011524280.1:p.Gly2843Asp
XM_011525979.1:c.8519G>A	XP_011524281.1:p.Gly2840Asp
XM_011525980.1:c.8510G>A	XP_011524282.1:p.Gly2837Asp
XM_011525981.1:c.8396G>A	XP_011524283.1:p.Gly2799Asp
XM_011525982.1:c.8231G>A	XP_011524284.1:p.Gly2744Asp
XM_011525978.2:c.8528G>A	XP_011524280.1:p.Gly2843Asp
XM_011525979.2:c.8519G>A	XP_011524281.1:p.Gly2840Asp
XM_011525980.2:c.8510G>A	XP_011524282.1:p.Gly2837Asp
XM_011525981.2:c.8396G>A	XP_011524283.1:p.Gly2799Asp
XM_011525982.2:c.8231G>A	XP_011524284.1:p.Gly2744Asp
XM_017025743.1:c.6380G>A	XP_016881232.1:p.Gly2127Asp
XM_017025744.1:c.4070G>A	XP_016881233.1:p.Gly1357Asp
XR_001753199.1:n.8769G>A
NM_000227.5:c.3674G>A	NP_000218.3:p.Gly1225Asp
NM_001127717.3:c.8333G>A	NP_001121189.2:p.Gly2778Asp
NM_001127718.3:c.3506G>A	NP_001121190.2:p.Gly1169Asp
NM_198129.3:c.8501G>A	NP_937762.2:p.Gly2834Asp
NM_000227.6:c.3674G>A MANE Plus Clinical	NP_000218.3:p.Gly1225Asp
NM_001127717.4:c.8333G>A	NP_001121189.2:p.Gly2778Asp
NM_001127718.4:c.3506G>A	NP_001121190.2:p.Gly1169Asp
NM_198129.4:c.8501G>A MANE Select	NP_937762.2:p.Gly2834Asp