Canonical Allele Identifier: CA402046463

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21478778A>G (hg19) ; chr18:g.23898814A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23898814A>G , CM000680.2:g.23898814A>G	GRCh38
NC_000018.9:g.21478778A>G , CM000680.1:g.21478778A>G	GRCh37
NC_000018.8:g.19732776A>G	NCBI36
NG_007853.2:g.214217A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.863A>G MANE Plus Clinical	ENSP00000269217.5:p.Asp288Gly
ENST00000313654.14:c.5690A>G MANE Select	ENSP00000324532.8:p.Asp1897Gly
ENST00000649721.1:c.2582A>G	ENSP00000497885.1:p.Asp861Gly
ENST00000269217.10:c.863A>G	ENSP00000269217.5:p.Asp288Gly
ENST00000313654.13:c.5690A>G	ENSP00000324532.8:p.Asp1897Gly
ENST00000399516.7:c.5690A>G	ENSP00000382432.2:p.Asp1897Gly
ENST00000586709.1:n.78A>G
ENST00000586751.5:c.468A>G
ENST00000587184.5:c.863A>G	ENSP00000466557.1:p.Asp288Gly
ENST00000588770.5:n.268A>G
NM_000227.4:c.863A>G	NP_000218.3:p.Asp288Gly
NM_001127717.2:c.5690A>G	NP_001121189.2:p.Asp1897Gly
NM_001127718.2:c.863A>G	NP_001121190.2:p.Asp288Gly
NM_198129.2:c.5690A>G	NP_937762.2:p.Asp1897Gly
XM_011525978.1:c.5717A>G	XP_011524280.1:p.Asp1906Gly
XM_011525979.1:c.5708A>G	XP_011524281.1:p.Asp1903Gly
XM_011525980.1:c.5699A>G	XP_011524282.1:p.Asp1900Gly
XM_011525981.1:c.5585A>G	XP_011524283.1:p.Asp1862Gly
XM_011525982.1:c.5717A>G	XP_011524284.1:p.Asp1906Gly
XM_011525978.2:c.5717A>G	XP_011524280.1:p.Asp1906Gly
XM_011525979.2:c.5708A>G	XP_011524281.1:p.Asp1903Gly
XM_011525980.2:c.5699A>G	XP_011524282.1:p.Asp1900Gly
XM_011525981.2:c.5585A>G	XP_011524283.1:p.Asp1862Gly
XM_011525982.2:c.5717A>G	XP_011524284.1:p.Asp1906Gly
XM_017025743.1:c.3569A>G	XP_016881232.1:p.Asp1190Gly
XM_017025744.1:c.1259A>G	XP_016881233.1:p.Asp420Gly
XR_001753199.1:n.5958A>G
NM_000227.5:c.863A>G	NP_000218.3:p.Asp288Gly
NM_001127717.3:c.5690A>G	NP_001121189.2:p.Asp1897Gly
NM_001127718.3:c.863A>G	NP_001121190.2:p.Asp288Gly
NM_198129.3:c.5690A>G	NP_937762.2:p.Asp1897Gly
NM_000227.6:c.863A>G MANE Plus Clinical	NP_000218.3:p.Asp288Gly
NM_001127717.4:c.5690A>G	NP_001121189.2:p.Asp1897Gly
NM_001127718.4:c.863A>G	NP_001121190.2:p.Asp288Gly
NM_198129.4:c.5690A>G MANE Select	NP_937762.2:p.Asp1897Gly