Canonical Allele Identifier: CA402048694

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21482992A>G (hg19) ; chr18:g.23903028A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23903028A>G , CM000680.2:g.23903028A>G	GRCh38
NC_000018.9:g.21482992A>G , CM000680.1:g.21482992A>G	GRCh37
NC_000018.8:g.19736990A>G	NCBI36
NG_007853.2:g.218431A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1394A>G MANE Plus Clinical	ENSP00000269217.5:p.Asn465Ser
ENST00000313654.14:c.6221A>G MANE Select	ENSP00000324532.8:p.Asn2074Ser
ENST00000649721.1:c.3113A>G	ENSP00000497885.1:p.Asn1038Ser
ENST00000269217.10:c.1394A>G	ENSP00000269217.5:p.Asn465Ser
ENST00000313654.13:c.6221A>G	ENSP00000324532.8:p.Asn2074Ser
ENST00000399516.7:c.6053A>G	ENSP00000382432.2:p.Asn2018Ser
ENST00000586751.5:c.999A>G
ENST00000587184.5:c.1226A>G	ENSP00000466557.1:p.Asn409Ser
ENST00000588770.5:n.799A>G
NM_000227.4:c.1394A>G	NP_000218.3:p.Asn465Ser
NM_001127717.2:c.6053A>G	NP_001121189.2:p.Asn2018Ser
NM_001127718.2:c.1226A>G	NP_001121190.2:p.Asn409Ser
NM_198129.2:c.6221A>G	NP_937762.2:p.Asn2074Ser
XM_011525978.1:c.6248A>G	XP_011524280.1:p.Asn2083Ser
XM_011525979.1:c.6239A>G	XP_011524281.1:p.Asn2080Ser
XM_011525980.1:c.6230A>G	XP_011524282.1:p.Asn2077Ser
XM_011525981.1:c.6116A>G	XP_011524283.1:p.Asn2039Ser
XM_011525982.1:c.6248A>G	XP_011524284.1:p.Asn2083Ser
XM_011525978.2:c.6248A>G	XP_011524280.1:p.Asn2083Ser
XM_011525979.2:c.6239A>G	XP_011524281.1:p.Asn2080Ser
XM_011525980.2:c.6230A>G	XP_011524282.1:p.Asn2077Ser
XM_011525981.2:c.6116A>G	XP_011524283.1:p.Asn2039Ser
XM_011525982.2:c.6248A>G	XP_011524284.1:p.Asn2083Ser
XM_017025743.1:c.4100A>G	XP_016881232.1:p.Asn1367Ser
XM_017025744.1:c.1790A>G	XP_016881233.1:p.Asn597Ser
XR_001753199.1:n.6489A>G
NM_000227.5:c.1394A>G	NP_000218.3:p.Asn465Ser
NM_001127717.3:c.6053A>G	NP_001121189.2:p.Asn2018Ser
NM_001127718.3:c.1226A>G	NP_001121190.2:p.Asn409Ser
NM_198129.3:c.6221A>G	NP_937762.2:p.Asn2074Ser
NM_000227.6:c.1394A>G MANE Plus Clinical	NP_000218.3:p.Asn465Ser
NM_001127717.4:c.6053A>G	NP_001121189.2:p.Asn2018Ser
NM_001127718.4:c.1226A>G	NP_001121190.2:p.Asn409Ser
NM_198129.4:c.6221A>G MANE Select	NP_937762.2:p.Asn2074Ser