Canonical Allele Identifier: CA297102457

Gene: LAMA3

Linked Data

• dbSNP Id: rs1014884895
• gnomAD v2: 18-21484308-A-G
• gnomAD v3: 18-23904344-A-G
• gnomAD v4: 18-23904344-A-G
• MyVariant Identifiers: chr18:g.21484308A>G (hg19) ; chr18:g.23904344A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23904344A>G , CM000680.2:g.23904344A>G	GRCh38
NC_000018.9:g.21484308A>G , CM000680.1:g.21484308A>G	GRCh37
NC_000018.8:g.19738306A>G	NCBI36
NG_007853.2:g.219747A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1647-209A>G MANE Plus Clinical	ENSP00000269217.5:n.1647-209A>G
ENST00000313654.14:c.6474-209A>G MANE Select	ENSP00000324532.8:n.6474-209A>G
ENST00000649721.1:c.3366-209A>G	ENSP00000497885.1:n.3366-209A>G
ENST00000269217.10:c.1647-209A>G	ENSP00000269217.5:n.1647-209A>G
ENST00000313654.13:c.6474-209A>G	ENSP00000324532.8:n.6474-209A>G
ENST00000399516.7:c.6306-209A>G	ENSP00000382432.2:n.6306-209A>G
ENST00000586751.5:c.1252-209A>G
ENST00000587184.5:c.1479-209A>G	ENSP00000466557.1:n.1479-209A>G
ENST00000588770.5:n.1052-209A>G
NM_000227.4:c.1647-209A>G	NP_000218.3:n.1647-209A>G
NM_001127717.2:c.6306-209A>G	NP_001121189.2:n.6306-209A>G
NM_001127718.2:c.1479-209A>G	NP_001121190.2:n.1479-209A>G
NM_198129.2:c.6474-209A>G	NP_937762.2:n.6474-209A>G
XM_011525978.1:c.6501-209A>G	XP_011524280.1:n.6501-209A>G
XM_011525979.1:c.6492-209A>G	XP_011524281.1:n.6492-209A>G
XM_011525980.1:c.6483-209A>G	XP_011524282.1:n.6483-209A>G
XM_011525981.1:c.6369-209A>G	XP_011524283.1:n.6369-209A>G
XM_011525982.1:c.6501-209A>G	XP_011524284.1:n.6501-209A>G
XM_011525978.2:c.6501-209A>G	XP_011524280.1:n.6501-209A>G
XM_011525979.2:c.6492-209A>G	XP_011524281.1:n.6492-209A>G
XM_011525980.2:c.6483-209A>G	XP_011524282.1:n.6483-209A>G
XM_011525981.2:c.6369-209A>G	XP_011524283.1:n.6369-209A>G
XM_011525982.2:c.6501-209A>G	XP_011524284.1:n.6501-209A>G
XM_017025743.1:c.4353-209A>G	XP_016881232.1:n.4353-209A>G
XM_017025744.1:c.2043-209A>G	XP_016881233.1:n.2043-209A>G
XR_001753199.1:n.6742-209A>G
NM_000227.5:c.1647-209A>G	NP_000218.3:n.1647-209A>G
NM_001127717.3:c.6306-209A>G	NP_001121189.2:n.6306-209A>G
NM_001127718.3:c.1479-209A>G	NP_001121190.2:n.1479-209A>G
NM_198129.3:c.6474-209A>G	NP_937762.2:n.6474-209A>G
NM_000227.6:c.1647-209A>G MANE Plus Clinical	NP_000218.3:n.1647-209A>G
NM_001127717.4:c.6306-209A>G	NP_001121189.2:n.6306-209A>G
NM_001127718.4:c.1479-209A>G	NP_001121190.2:n.1479-209A>G
NM_198129.4:c.6474-209A>G MANE Select	NP_937762.2:n.6474-209A>G