Canonical Allele Identifier: CA2290334627

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928209G= , CM000680.2:g.23928209G=	GRCh38
NC_000018.9:g.21508173G= , CM000680.1:g.21508173G=	GRCh37
NC_000018.8:g.19762171G=	NCBI36
NG_007853.2:g.243612G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3437G= MANE Plus Clinical	ENSP00000269217.5:p.Gly1146=
ENST00000313654.14:c.8264G= MANE Select	ENSP00000324532.8:p.Gly2755=
ENST00000649721.1:c.4859G=	ENSP00000497885.1:p.Gly1620=
ENST00000269217.10:c.3437G=	ENSP00000269217.5:p.Gly1146=
ENST00000313654.13:c.8264G=	ENSP00000324532.8:p.Gly2755=
ENST00000399516.7:c.8096G=	ENSP00000382432.2:p.Gly2699=
ENST00000586751.5:c.3042G=
ENST00000587184.5:c.3269G=	ENSP00000466557.1:p.Gly1090=
ENST00000588770.5:n.2842G=
NM_000227.4:c.3437G=	NP_000218.3:p.Gly1146=
NM_001127717.2:c.8096G=	NP_001121189.2:p.Gly2699=
NM_001127718.2:c.3269G=	NP_001121190.2:p.Gly1090=
NM_198129.2:c.8264G=	NP_937762.2:p.Gly2755=
XM_011525978.1:c.8291G=	XP_011524280.1:p.Gly2764=
XM_011525979.1:c.8282G=	XP_011524281.1:p.Gly2761=
XM_011525980.1:c.8273G=	XP_011524282.1:p.Gly2758=
XM_011525981.1:c.8159G=	XP_011524283.1:p.Gly2720=
XM_011525982.1:c.7994G=	XP_011524284.1:p.Gly2665=
XM_011525978.2:c.8291G=	XP_011524280.1:p.Gly2764=
XM_011525979.2:c.8282G=	XP_011524281.1:p.Gly2761=
XM_011525980.2:c.8273G=	XP_011524282.1:p.Gly2758=
XM_011525981.2:c.8159G=	XP_011524283.1:p.Gly2720=
XM_011525982.2:c.7994G=	XP_011524284.1:p.Gly2665=
XM_017025743.1:c.6143G=	XP_016881232.1:p.Gly2048=
XM_017025744.1:c.3833G=	XP_016881233.1:p.Gly1278=
XR_001753199.1:n.8532G=
NM_000227.5:c.3437G=	NP_000218.3:p.Gly1146=
NM_001127717.3:c.8096G=	NP_001121189.2:p.Gly2699=
NM_001127718.3:c.3269G=	NP_001121190.2:p.Gly1090=
NM_198129.3:c.8264G=	NP_937762.2:p.Gly2755=
NM_000227.6:c.3437G= MANE Plus Clinical	NP_000218.3:p.Gly1146=
NM_001127717.4:c.8096G=	NP_001121189.2:p.Gly2699=
NM_001127718.4:c.3269G=	NP_001121190.2:p.Gly1090=
NM_198129.4:c.8264G= MANE Select	NP_937762.2:p.Gly2755=