Canonical Allele Identifier: CA402045093

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21456370T>A (hg19) ; chr18:g.23876406T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23876406T>A , CM000680.2:g.23876406T>A	GRCh38
NC_000018.9:g.21456370T>A , CM000680.1:g.21456370T>A	GRCh37
NC_000018.8:g.19710368T>A	NCBI36
NG_007853.2:g.191809T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.284T>A MANE Plus Clinical	ENSP00000269217.5:p.Val95Asp
ENST00000313654.14:c.5111T>A MANE Select	ENSP00000324532.8:p.Val1704Asp
ENST00000649721.1:c.2003T>A	ENSP00000497885.1:p.Val668Asp
ENST00000269217.10:c.284T>A	ENSP00000269217.5:p.Val95Asp
ENST00000313654.13:c.5111T>A	ENSP00000324532.8:p.Val1704Asp
ENST00000399516.7:c.5111T>A	ENSP00000382432.2:p.Val1704Asp
ENST00000587184.5:c.284T>A	ENSP00000466557.1:p.Val95Asp
NM_000227.4:c.284T>A	NP_000218.3:p.Val95Asp
NM_001127717.2:c.5111T>A	NP_001121189.2:p.Val1704Asp
NM_001127718.2:c.284T>A	NP_001121190.2:p.Val95Asp
NM_198129.2:c.5111T>A	NP_937762.2:p.Val1704Asp
XM_011525978.1:c.5138T>A	XP_011524280.1:p.Val1713Asp
XM_011525979.1:c.5129T>A	XP_011524281.1:p.Val1710Asp
XM_011525980.1:c.5120T>A	XP_011524282.1:p.Val1707Asp
XM_011525981.1:c.5006T>A	XP_011524283.1:p.Val1669Asp
XM_011525982.1:c.5138T>A	XP_011524284.1:p.Val1713Asp
XM_011525978.2:c.5138T>A	XP_011524280.1:p.Val1713Asp
XM_011525979.2:c.5129T>A	XP_011524281.1:p.Val1710Asp
XM_011525980.2:c.5120T>A	XP_011524282.1:p.Val1707Asp
XM_011525981.2:c.5006T>A	XP_011524283.1:p.Val1669Asp
XM_011525982.2:c.5138T>A	XP_011524284.1:p.Val1713Asp
XM_017025743.1:c.2990T>A	XP_016881232.1:p.Val997Asp
XM_017025744.1:c.680T>A	XP_016881233.1:p.Val227Asp
XR_001753199.1:n.5379T>A
NM_000227.5:c.284T>A	NP_000218.3:p.Val95Asp
NM_001127717.3:c.5111T>A	NP_001121189.2:p.Val1704Asp
NM_001127718.3:c.284T>A	NP_001121190.2:p.Val95Asp
NM_198129.3:c.5111T>A	NP_937762.2:p.Val1704Asp
NM_000227.6:c.284T>A MANE Plus Clinical	NP_000218.3:p.Val95Asp
NM_001127717.4:c.5111T>A	NP_001121189.2:p.Val1704Asp
NM_001127718.4:c.284T>A	NP_001121190.2:p.Val95Asp
NM_198129.4:c.5111T>A MANE Select	NP_937762.2:p.Val1704Asp