Canonical Allele Identifier: CA402063214

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21508158T>A (hg19) ; chr18:g.23928194T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928194T>A , CM000680.2:g.23928194T>A	GRCh38
NC_000018.9:g.21508158T>A , CM000680.1:g.21508158T>A	GRCh37
NC_000018.8:g.19762156T>A	NCBI36
NG_007853.2:g.243597T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3422T>A MANE Plus Clinical	ENSP00000269217.5:p.Leu1141Ter
ENST00000313654.14:c.8249T>A MANE Select	ENSP00000324532.8:p.Leu2750Ter
ENST00000649721.1:c.4844T>A	ENSP00000497885.1:p.Leu1615Ter
ENST00000269217.10:c.3422T>A	ENSP00000269217.5:p.Leu1141Ter
ENST00000313654.13:c.8249T>A	ENSP00000324532.8:p.Leu2750Ter
ENST00000399516.7:c.8081T>A	ENSP00000382432.2:p.Leu2694Ter
ENST00000586751.5:c.3027T>A
ENST00000587184.5:c.3254T>A	ENSP00000466557.1:p.Leu1085Ter
ENST00000588770.5:n.2827T>A
NM_000227.4:c.3422T>A	NP_000218.3:p.Leu1141Ter
NM_001127717.2:c.8081T>A	NP_001121189.2:p.Leu2694Ter
NM_001127718.2:c.3254T>A	NP_001121190.2:p.Leu1085Ter
NM_198129.2:c.8249T>A	NP_937762.2:p.Leu2750Ter
XM_011525978.1:c.8276T>A	XP_011524280.1:p.Leu2759Ter
XM_011525979.1:c.8267T>A	XP_011524281.1:p.Leu2756Ter
XM_011525980.1:c.8258T>A	XP_011524282.1:p.Leu2753Ter
XM_011525981.1:c.8144T>A	XP_011524283.1:p.Leu2715Ter
XM_011525982.1:c.7979T>A	XP_011524284.1:p.Leu2660Ter
XM_011525978.2:c.8276T>A	XP_011524280.1:p.Leu2759Ter
XM_011525979.2:c.8267T>A	XP_011524281.1:p.Leu2756Ter
XM_011525980.2:c.8258T>A	XP_011524282.1:p.Leu2753Ter
XM_011525981.2:c.8144T>A	XP_011524283.1:p.Leu2715Ter
XM_011525982.2:c.7979T>A	XP_011524284.1:p.Leu2660Ter
XM_017025743.1:c.6128T>A	XP_016881232.1:p.Leu2043Ter
XM_017025744.1:c.3818T>A	XP_016881233.1:p.Leu1273Ter
XR_001753199.1:n.8517T>A
NM_000227.5:c.3422T>A	NP_000218.3:p.Leu1141Ter
NM_001127717.3:c.8081T>A	NP_001121189.2:p.Leu2694Ter
NM_001127718.3:c.3254T>A	NP_001121190.2:p.Leu1085Ter
NM_198129.3:c.8249T>A	NP_937762.2:p.Leu2750Ter
NM_000227.6:c.3422T>A MANE Plus Clinical	NP_000218.3:p.Leu1141Ter
NM_001127717.4:c.8081T>A	NP_001121189.2:p.Leu2694Ter
NM_001127718.4:c.3254T>A	NP_001121190.2:p.Leu1085Ter
NM_198129.4:c.8249T>A MANE Select	NP_937762.2:p.Leu2750Ter