Canonical Allele Identifier: CA402051297

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21485501G>T (hg19) ; chr18:g.23905537G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23905537G>T , CM000680.2:g.23905537G>T	GRCh38
NC_000018.9:g.21485501G>T , CM000680.1:g.21485501G>T	GRCh37
NC_000018.8:g.19739499G>T	NCBI36
NG_007853.2:g.220940G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1804G>T MANE Plus Clinical	ENSP00000269217.5:p.Asp602Tyr
ENST00000313654.14:c.6631G>T MANE Select	ENSP00000324532.8:p.Asp2211Tyr
ENST00000649721.1:c.3523G>T	ENSP00000497885.1:p.Asp1175Tyr
ENST00000269217.10:c.1804G>T	ENSP00000269217.5:p.Asp602Tyr
ENST00000313654.13:c.6631G>T	ENSP00000324532.8:p.Asp2211Tyr
ENST00000399516.7:c.6463G>T	ENSP00000382432.2:p.Asp2155Tyr
ENST00000586751.5:c.1409G>T
ENST00000587184.5:c.1636G>T	ENSP00000466557.1:p.Asp546Tyr
ENST00000588770.5:n.1209G>T
NM_000227.4:c.1804G>T	NP_000218.3:p.Asp602Tyr
NM_001127717.2:c.6463G>T	NP_001121189.2:p.Asp2155Tyr
NM_001127718.2:c.1636G>T	NP_001121190.2:p.Asp546Tyr
NM_198129.2:c.6631G>T	NP_937762.2:p.Asp2211Tyr
XM_011525978.1:c.6658G>T	XP_011524280.1:p.Asp2220Tyr
XM_011525979.1:c.6649G>T	XP_011524281.1:p.Asp2217Tyr
XM_011525980.1:c.6640G>T	XP_011524282.1:p.Asp2214Tyr
XM_011525981.1:c.6526G>T	XP_011524283.1:p.Asp2176Tyr
XM_011525982.1:c.6658G>T	XP_011524284.1:p.Asp2220Tyr
XM_011525978.2:c.6658G>T	XP_011524280.1:p.Asp2220Tyr
XM_011525979.2:c.6649G>T	XP_011524281.1:p.Asp2217Tyr
XM_011525980.2:c.6640G>T	XP_011524282.1:p.Asp2214Tyr
XM_011525981.2:c.6526G>T	XP_011524283.1:p.Asp2176Tyr
XM_011525982.2:c.6658G>T	XP_011524284.1:p.Asp2220Tyr
XM_017025743.1:c.4510G>T	XP_016881232.1:p.Asp1504Tyr
XM_017025744.1:c.2200G>T	XP_016881233.1:p.Asp734Tyr
XR_001753199.1:n.6899G>T
NM_000227.5:c.1804G>T	NP_000218.3:p.Asp602Tyr
NM_001127717.3:c.6463G>T	NP_001121189.2:p.Asp2155Tyr
NM_001127718.3:c.1636G>T	NP_001121190.2:p.Asp546Tyr
NM_198129.3:c.6631G>T	NP_937762.2:p.Asp2211Tyr
NM_000227.6:c.1804G>T MANE Plus Clinical	NP_000218.3:p.Asp602Tyr
NM_001127717.4:c.6463G>T	NP_001121189.2:p.Asp2155Tyr
NM_001127718.4:c.1636G>T	NP_001121190.2:p.Asp546Tyr
NM_198129.4:c.6631G>T MANE Select	NP_937762.2:p.Asp2211Tyr