Canonical Allele Identifier: CA628979082

Gene: LAMA3

Linked Data

• dbSNP Id: rs1239746671
• gnomAD v2: 18-21479033-A-G
• gnomAD v3: 18-23899069-A-G
• gnomAD v4: 18-23899069-A-G
• MyVariant Identifiers: chr18:g.21479033A>G (hg19) ; chr18:g.23899069A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23899069A>G , CM000680.2:g.23899069A>G	GRCh38
NC_000018.9:g.21479033A>G , CM000680.1:g.21479033A>G	GRCh37
NC_000018.8:g.19733031A>G	NCBI36
NG_007853.2:g.214472A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.1009+4A>G MANE Plus Clinical	ENSP00000269217.5:n.1009+4A>G
ENST00000313654.14:c.5836+4A>G MANE Select	ENSP00000324532.8:n.5836+4A>G
ENST00000649721.1:c.2728+4A>G	ENSP00000497885.1:n.2728+4A>G
ENST00000269217.10:c.1009+4A>G	ENSP00000269217.5:n.1009+4A>G
ENST00000313654.13:c.5836+4A>G	ENSP00000324532.8:n.5836+4A>G
ENST00000399516.7:c.5836+4A>G	ENSP00000382432.2:n.5836+4A>G
ENST00000586709.1:n.224+4A>G
ENST00000586751.5:c.614+4A>G
ENST00000587184.5:c.1009+4A>G	ENSP00000466557.1:n.1009+4A>G
ENST00000588770.5:n.414+4A>G
NM_000227.4:c.1009+4A>G	NP_000218.3:n.1009+4A>G
NM_001127717.2:c.5836+4A>G	NP_001121189.2:n.5836+4A>G
NM_001127718.2:c.1009+4A>G	NP_001121190.2:n.1009+4A>G
NM_198129.2:c.5836+4A>G	NP_937762.2:n.5836+4A>G
XM_011525978.1:c.5863+4A>G	XP_011524280.1:n.5863+4A>G
XM_011525979.1:c.5854+4A>G	XP_011524281.1:n.5854+4A>G
XM_011525980.1:c.5845+4A>G	XP_011524282.1:n.5845+4A>G
XM_011525981.1:c.5731+4A>G	XP_011524283.1:n.5731+4A>G
XM_011525982.1:c.5863+4A>G	XP_011524284.1:n.5863+4A>G
XM_011525978.2:c.5863+4A>G	XP_011524280.1:n.5863+4A>G
XM_011525979.2:c.5854+4A>G	XP_011524281.1:n.5854+4A>G
XM_011525980.2:c.5845+4A>G	XP_011524282.1:n.5845+4A>G
XM_011525981.2:c.5731+4A>G	XP_011524283.1:n.5731+4A>G
XM_011525982.2:c.5863+4A>G	XP_011524284.1:n.5863+4A>G
XM_017025743.1:c.3715+4A>G	XP_016881232.1:n.3715+4A>G
XM_017025744.1:c.1405+4A>G	XP_016881233.1:n.1405+4A>G
XR_001753199.1:n.6104+4A>G
NM_000227.5:c.1009+4A>G	NP_000218.3:n.1009+4A>G
NM_001127717.3:c.5836+4A>G	NP_001121189.2:n.5836+4A>G
NM_001127718.3:c.1009+4A>G	NP_001121190.2:n.1009+4A>G
NM_198129.3:c.5836+4A>G	NP_937762.2:n.5836+4A>G
NM_000227.6:c.1009+4A>G MANE Plus Clinical	NP_000218.3:n.1009+4A>G
NM_001127717.4:c.5836+4A>G	NP_001121189.2:n.5836+4A>G
NM_001127718.4:c.1009+4A>G	NP_001121190.2:n.1009+4A>G
NM_198129.4:c.5836+4A>G MANE Select	NP_937762.2:n.5836+4A>G