Canonical Allele Identifier: CA402063260

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21508166A>G (hg19) ; chr18:g.23928202A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928202A>G , CM000680.2:g.23928202A>G	GRCh38
NC_000018.9:g.21508166A>G , CM000680.1:g.21508166A>G	GRCh37
NC_000018.8:g.19762164A>G	NCBI36
NG_007853.2:g.243605A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3430A>G MANE Plus Clinical	ENSP00000269217.5:p.Thr1144Ala
ENST00000313654.14:c.8257A>G MANE Select	ENSP00000324532.8:p.Thr2753Ala
ENST00000649721.1:c.4852A>G	ENSP00000497885.1:p.Thr1618Ala
ENST00000269217.10:c.3430A>G	ENSP00000269217.5:p.Thr1144Ala
ENST00000313654.13:c.8257A>G	ENSP00000324532.8:p.Thr2753Ala
ENST00000399516.7:c.8089A>G	ENSP00000382432.2:p.Thr2697Ala
ENST00000586751.5:c.3035A>G
ENST00000587184.5:c.3262A>G	ENSP00000466557.1:p.Thr1088Ala
ENST00000588770.5:n.2835A>G
NM_000227.4:c.3430A>G	NP_000218.3:p.Thr1144Ala
NM_001127717.2:c.8089A>G	NP_001121189.2:p.Thr2697Ala
NM_001127718.2:c.3262A>G	NP_001121190.2:p.Thr1088Ala
NM_198129.2:c.8257A>G	NP_937762.2:p.Thr2753Ala
XM_011525978.1:c.8284A>G	XP_011524280.1:p.Thr2762Ala
XM_011525979.1:c.8275A>G	XP_011524281.1:p.Thr2759Ala
XM_011525980.1:c.8266A>G	XP_011524282.1:p.Thr2756Ala
XM_011525981.1:c.8152A>G	XP_011524283.1:p.Thr2718Ala
XM_011525982.1:c.7987A>G	XP_011524284.1:p.Thr2663Ala
XM_011525978.2:c.8284A>G	XP_011524280.1:p.Thr2762Ala
XM_011525979.2:c.8275A>G	XP_011524281.1:p.Thr2759Ala
XM_011525980.2:c.8266A>G	XP_011524282.1:p.Thr2756Ala
XM_011525981.2:c.8152A>G	XP_011524283.1:p.Thr2718Ala
XM_011525982.2:c.7987A>G	XP_011524284.1:p.Thr2663Ala
XM_017025743.1:c.6136A>G	XP_016881232.1:p.Thr2046Ala
XM_017025744.1:c.3826A>G	XP_016881233.1:p.Thr1276Ala
XR_001753199.1:n.8525A>G
NM_000227.5:c.3430A>G	NP_000218.3:p.Thr1144Ala
NM_001127717.3:c.8089A>G	NP_001121189.2:p.Thr2697Ala
NM_001127718.3:c.3262A>G	NP_001121190.2:p.Thr1088Ala
NM_198129.3:c.8257A>G	NP_937762.2:p.Thr2753Ala
NM_000227.6:c.3430A>G MANE Plus Clinical	NP_000218.3:p.Thr1144Ala
NM_001127717.4:c.8089A>G	NP_001121189.2:p.Thr2697Ala
NM_001127718.4:c.3262A>G	NP_001121190.2:p.Thr1088Ala
NM_198129.4:c.8257A>G MANE Select	NP_937762.2:p.Thr2753Ala