Canonical Allele Identifier: CA402063168

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21508148G>C (hg19) ; chr18:g.23928184G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928184G>C , CM000680.2:g.23928184G>C	GRCh38
NC_000018.9:g.21508148G>C , CM000680.1:g.21508148G>C	GRCh37
NC_000018.8:g.19762146G>C	NCBI36
NG_007853.2:g.243587G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3412G>C MANE Plus Clinical	ENSP00000269217.5:p.Val1138Leu
ENST00000313654.14:c.8239G>C MANE Select	ENSP00000324532.8:p.Val2747Leu
ENST00000649721.1:c.4834G>C	ENSP00000497885.1:p.Val1612Leu
ENST00000269217.10:c.3412G>C	ENSP00000269217.5:p.Val1138Leu
ENST00000313654.13:c.8239G>C	ENSP00000324532.8:p.Val2747Leu
ENST00000399516.7:c.8071G>C	ENSP00000382432.2:p.Val2691Leu
ENST00000586751.5:c.3017G>C
ENST00000587184.5:c.3244G>C	ENSP00000466557.1:p.Val1082Leu
ENST00000588770.5:n.2817G>C
NM_000227.4:c.3412G>C	NP_000218.3:p.Val1138Leu
NM_001127717.2:c.8071G>C	NP_001121189.2:p.Val2691Leu
NM_001127718.2:c.3244G>C	NP_001121190.2:p.Val1082Leu
NM_198129.2:c.8239G>C	NP_937762.2:p.Val2747Leu
XM_011525978.1:c.8266G>C	XP_011524280.1:p.Val2756Leu
XM_011525979.1:c.8257G>C	XP_011524281.1:p.Val2753Leu
XM_011525980.1:c.8248G>C	XP_011524282.1:p.Val2750Leu
XM_011525981.1:c.8134G>C	XP_011524283.1:p.Val2712Leu
XM_011525982.1:c.7969G>C	XP_011524284.1:p.Val2657Leu
XM_011525978.2:c.8266G>C	XP_011524280.1:p.Val2756Leu
XM_011525979.2:c.8257G>C	XP_011524281.1:p.Val2753Leu
XM_011525980.2:c.8248G>C	XP_011524282.1:p.Val2750Leu
XM_011525981.2:c.8134G>C	XP_011524283.1:p.Val2712Leu
XM_011525982.2:c.7969G>C	XP_011524284.1:p.Val2657Leu
XM_017025743.1:c.6118G>C	XP_016881232.1:p.Val2040Leu
XM_017025744.1:c.3808G>C	XP_016881233.1:p.Val1270Leu
XR_001753199.1:n.8507G>C
NM_000227.5:c.3412G>C	NP_000218.3:p.Val1138Leu
NM_001127717.3:c.8071G>C	NP_001121189.2:p.Val2691Leu
NM_001127718.3:c.3244G>C	NP_001121190.2:p.Val1082Leu
NM_198129.3:c.8239G>C	NP_937762.2:p.Val2747Leu
NM_000227.6:c.3412G>C MANE Plus Clinical	NP_000218.3:p.Val1138Leu
NM_001127717.4:c.8071G>C	NP_001121189.2:p.Val2691Leu
NM_001127718.4:c.3244G>C	NP_001121190.2:p.Val1082Leu
NM_198129.4:c.8239G>C MANE Select	NP_937762.2:p.Val2747Leu