Canonical Allele Identifier: CA402048794

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21483020T>A (hg19) ; chr18:g.23903056T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23903056T>A , CM000680.2:g.23903056T>A	GRCh38
NC_000018.9:g.21483020T>A , CM000680.1:g.21483020T>A	GRCh37
NC_000018.8:g.19737018T>A	NCBI36
NG_007853.2:g.218459T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.1422T>A MANE Plus Clinical	ENSP00000269217.5:p.Tyr474Ter
ENST00000313654.14:c.6249T>A MANE Select	ENSP00000324532.8:p.Tyr2083Ter
ENST00000649721.1:c.3141T>A	ENSP00000497885.1:p.Tyr1047Ter
ENST00000269217.10:c.1422T>A	ENSP00000269217.5:p.Tyr474Ter
ENST00000313654.13:c.6249T>A	ENSP00000324532.8:p.Tyr2083Ter
ENST00000399516.7:c.6081T>A	ENSP00000382432.2:p.Tyr2027Ter
ENST00000586751.5:c.1027T>A
ENST00000587184.5:c.1254T>A	ENSP00000466557.1:p.Tyr418Ter
ENST00000588770.5:n.827T>A
NM_000227.4:c.1422T>A	NP_000218.3:p.Tyr474Ter
NM_001127717.2:c.6081T>A	NP_001121189.2:p.Tyr2027Ter
NM_001127718.2:c.1254T>A	NP_001121190.2:p.Tyr418Ter
NM_198129.2:c.6249T>A	NP_937762.2:p.Tyr2083Ter
XM_011525978.1:c.6276T>A	XP_011524280.1:p.Tyr2092Ter
XM_011525979.1:c.6267T>A	XP_011524281.1:p.Tyr2089Ter
XM_011525980.1:c.6258T>A	XP_011524282.1:p.Tyr2086Ter
XM_011525981.1:c.6144T>A	XP_011524283.1:p.Tyr2048Ter
XM_011525982.1:c.6276T>A	XP_011524284.1:p.Tyr2092Ter
XM_011525978.2:c.6276T>A	XP_011524280.1:p.Tyr2092Ter
XM_011525979.2:c.6267T>A	XP_011524281.1:p.Tyr2089Ter
XM_011525980.2:c.6258T>A	XP_011524282.1:p.Tyr2086Ter
XM_011525981.2:c.6144T>A	XP_011524283.1:p.Tyr2048Ter
XM_011525982.2:c.6276T>A	XP_011524284.1:p.Tyr2092Ter
XM_017025743.1:c.4128T>A	XP_016881232.1:p.Tyr1376Ter
XM_017025744.1:c.1818T>A	XP_016881233.1:p.Tyr606Ter
XR_001753199.1:n.6517T>A
NM_000227.5:c.1422T>A	NP_000218.3:p.Tyr474Ter
NM_001127717.3:c.6081T>A	NP_001121189.2:p.Tyr2027Ter
NM_001127718.3:c.1254T>A	NP_001121190.2:p.Tyr418Ter
NM_198129.3:c.6249T>A	NP_937762.2:p.Tyr2083Ter
NM_000227.6:c.1422T>A MANE Plus Clinical	NP_000218.3:p.Tyr474Ter
NM_001127717.4:c.6081T>A	NP_001121189.2:p.Tyr2027Ter
NM_001127718.4:c.1254T>A	NP_001121190.2:p.Tyr418Ter
NM_198129.4:c.6249T>A MANE Select	NP_937762.2:p.Tyr2083Ter