Canonical Allele Identifier: CA2290334638

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928237G= , CM000680.2:g.23928237G=	GRCh38
NC_000018.9:g.21508201G= , CM000680.1:g.21508201G=	GRCh37
NC_000018.8:g.19762199G=	NCBI36
NG_007853.2:g.243640G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3465G= MANE Plus Clinical	ENSP00000269217.5:p.Trp1155=
ENST00000313654.14:c.8292G= MANE Select	ENSP00000324532.8:p.Trp2764=
ENST00000649721.1:c.4887G=	ENSP00000497885.1:p.Trp1629=
ENST00000269217.10:c.3465G=	ENSP00000269217.5:p.Trp1155=
ENST00000313654.13:c.8292G=	ENSP00000324532.8:p.Trp2764=
ENST00000399516.7:c.8124G=	ENSP00000382432.2:p.Trp2708=
ENST00000586751.5:c.3070G=
ENST00000587184.5:c.3297G=	ENSP00000466557.1:p.Trp1099=
ENST00000588770.5:n.2870G=
NM_000227.4:c.3465G=	NP_000218.3:p.Trp1155=
NM_001127717.2:c.8124G=	NP_001121189.2:p.Trp2708=
NM_001127718.2:c.3297G=	NP_001121190.2:p.Trp1099=
NM_198129.2:c.8292G=	NP_937762.2:p.Trp2764=
XM_011525978.1:c.8319G=	XP_011524280.1:p.Trp2773=
XM_011525979.1:c.8310G=	XP_011524281.1:p.Trp2770=
XM_011525980.1:c.8301G=	XP_011524282.1:p.Trp2767=
XM_011525981.1:c.8187G=	XP_011524283.1:p.Trp2729=
XM_011525982.1:c.8022G=	XP_011524284.1:p.Trp2674=
XM_011525978.2:c.8319G=	XP_011524280.1:p.Trp2773=
XM_011525979.2:c.8310G=	XP_011524281.1:p.Trp2770=
XM_011525980.2:c.8301G=	XP_011524282.1:p.Trp2767=
XM_011525981.2:c.8187G=	XP_011524283.1:p.Trp2729=
XM_011525982.2:c.8022G=	XP_011524284.1:p.Trp2674=
XM_017025743.1:c.6171G=	XP_016881232.1:p.Trp2057=
XM_017025744.1:c.3861G=	XP_016881233.1:p.Trp1287=
XR_001753199.1:n.8560G=
NM_000227.5:c.3465G=	NP_000218.3:p.Trp1155=
NM_001127717.3:c.8124G=	NP_001121189.2:p.Trp2708=
NM_001127718.3:c.3297G=	NP_001121190.2:p.Trp1099=
NM_198129.3:c.8292G=	NP_937762.2:p.Trp2764=
NM_000227.6:c.3465G= MANE Plus Clinical	NP_000218.3:p.Trp1155=
NM_001127717.4:c.8124G=	NP_001121189.2:p.Trp2708=
NM_001127718.4:c.3297G=	NP_001121190.2:p.Trp1099=
NM_198129.4:c.8292G= MANE Select	NP_937762.2:p.Trp2764=