Canonical Allele Identifier: CA402044906

Gene: LAMA3

Linked Data

• gnomAD v4: 18-23876321-C-G
• MyVariant Identifiers: chr18:g.21456285C>G (hg19) ; chr18:g.23876321C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23876321C>G , CM000680.2:g.23876321C>G	GRCh38
NC_000018.9:g.21456285C>G , CM000680.1:g.21456285C>G	GRCh37
NC_000018.8:g.19710283C>G	NCBI36
NG_007853.2:g.191724C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.199C>G MANE Plus Clinical	ENSP00000269217.5:p.His67Asp
ENST00000313654.14:c.5026C>G MANE Select	ENSP00000324532.8:p.His1676Asp
ENST00000649721.1:c.1918C>G	ENSP00000497885.1:p.His640Asp
ENST00000269217.10:c.199C>G	ENSP00000269217.5:p.His67Asp
ENST00000313654.13:c.5026C>G	ENSP00000324532.8:p.His1676Asp
ENST00000399516.7:c.5026C>G	ENSP00000382432.2:p.His1676Asp
ENST00000587184.5:c.199C>G	ENSP00000466557.1:p.His67Asp
NM_000227.4:c.199C>G	NP_000218.3:p.His67Asp
NM_001127717.2:c.5026C>G	NP_001121189.2:p.His1676Asp
NM_001127718.2:c.199C>G	NP_001121190.2:p.His67Asp
NM_198129.2:c.5026C>G	NP_937762.2:p.His1676Asp
XM_011525978.1:c.5053C>G	XP_011524280.1:p.His1685Asp
XM_011525979.1:c.5044C>G	XP_011524281.1:p.His1682Asp
XM_011525980.1:c.5035C>G	XP_011524282.1:p.His1679Asp
XM_011525981.1:c.4921C>G	XP_011524283.1:p.His1641Asp
XM_011525982.1:c.5053C>G	XP_011524284.1:p.His1685Asp
XM_011525978.2:c.5053C>G	XP_011524280.1:p.His1685Asp
XM_011525979.2:c.5044C>G	XP_011524281.1:p.His1682Asp
XM_011525980.2:c.5035C>G	XP_011524282.1:p.His1679Asp
XM_011525981.2:c.4921C>G	XP_011524283.1:p.His1641Asp
XM_011525982.2:c.5053C>G	XP_011524284.1:p.His1685Asp
XM_017025743.1:c.2905C>G	XP_016881232.1:p.His969Asp
XM_017025744.1:c.595C>G	XP_016881233.1:p.His199Asp
XR_001753199.1:n.5294C>G
NM_000227.5:c.199C>G	NP_000218.3:p.His67Asp
NM_001127717.3:c.5026C>G	NP_001121189.2:p.His1676Asp
NM_001127718.3:c.199C>G	NP_001121190.2:p.His67Asp
NM_198129.3:c.5026C>G	NP_937762.2:p.His1676Asp
NM_000227.6:c.199C>G MANE Plus Clinical	NP_000218.3:p.His67Asp
NM_001127717.4:c.5026C>G	NP_001121189.2:p.His1676Asp
NM_001127718.4:c.199C>G	NP_001121190.2:p.His67Asp
NM_198129.4:c.5026C>G MANE Select	NP_937762.2:p.His1676Asp