Canonical Allele Identifier: CA503340631

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21508135G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928171G>A , CM000680.2:g.23928171G>A	GRCh38
NC_000018.9:g.21508135G>A , CM000680.1:g.21508135G>A	GRCh37
NC_000018.8:g.19762133G>A	NCBI36
NG_007853.2:g.243574G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3399G>A MANE Plus Clinical	ENSP00000269217.5:p.Lys1133=
ENST00000313654.14:c.8226G>A MANE Select	ENSP00000324532.8:p.Lys2742=
ENST00000649721.1:c.4821G>A	ENSP00000497885.1:p.Lys1607=
ENST00000269217.10:c.3399G>A	ENSP00000269217.5:p.Lys1133=
ENST00000313654.13:c.8226G>A	ENSP00000324532.8:p.Lys2742=
ENST00000399516.7:c.8058G>A	ENSP00000382432.2:p.Lys2686=
ENST00000586751.5:c.3004G>A
ENST00000587184.5:c.3231G>A	ENSP00000466557.1:p.Lys1077=
ENST00000588770.5:n.2804G>A
NM_000227.4:c.3399G>A	NP_000218.3:p.Lys1133=
NM_001127717.2:c.8058G>A	NP_001121189.2:p.Lys2686=
NM_001127718.2:c.3231G>A	NP_001121190.2:p.Lys1077=
NM_198129.2:c.8226G>A	NP_937762.2:p.Lys2742=
XM_011525978.1:c.8253G>A	XP_011524280.1:p.Lys2751=
XM_011525979.1:c.8244G>A	XP_011524281.1:p.Lys2748=
XM_011525980.1:c.8235G>A	XP_011524282.1:p.Lys2745=
XM_011525981.1:c.8121G>A	XP_011524283.1:p.Lys2707=
XM_011525982.1:c.7956G>A	XP_011524284.1:p.Lys2652=
XM_011525978.2:c.8253G>A	XP_011524280.1:p.Lys2751=
XM_011525979.2:c.8244G>A	XP_011524281.1:p.Lys2748=
XM_011525980.2:c.8235G>A	XP_011524282.1:p.Lys2745=
XM_011525981.2:c.8121G>A	XP_011524283.1:p.Lys2707=
XM_011525982.2:c.7956G>A	XP_011524284.1:p.Lys2652=
XM_017025743.1:c.6105G>A	XP_016881232.1:p.Lys2035=
XM_017025744.1:c.3795G>A	XP_016881233.1:p.Lys1265=
XR_001753199.1:n.8494G>A
NM_000227.5:c.3399G>A	NP_000218.3:p.Lys1133=
NM_001127717.3:c.8058G>A	NP_001121189.2:p.Lys2686=
NM_001127718.3:c.3231G>A	NP_001121190.2:p.Lys1077=
NM_198129.3:c.8226G>A	NP_937762.2:p.Lys2742=
NM_000227.6:c.3399G>A MANE Plus Clinical	NP_000218.3:p.Lys1133=
NM_001127717.4:c.8058G>A	NP_001121189.2:p.Lys2686=
NM_001127718.4:c.3231G>A	NP_001121190.2:p.Lys1077=
NM_198129.4:c.8226G>A MANE Select	NP_937762.2:p.Lys2742=