Canonical Allele Identifier: CA2290314742

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23882028A= , CM000680.2:g.23882028A=	GRCh38
NC_000018.9:g.21461992A= , CM000680.1:g.21461992A=	GRCh37
NC_000018.8:g.19715990A=	NCBI36
NG_007853.2:g.197431A=

Transcript Alleles

HGVS	Amino-acid Change
NM_198129.4:c.5205A= MANE Select	NP_937762.2:p.Pro1735=
ENST00000313654.14:c.5205A= MANE Select	ENSP00000324532.8:p.Pro1735=
NM_000227.6:c.378A= MANE Plus Clinical	NP_000218.3:p.Pro126=
ENST00000269217.11:c.378A= MANE Plus Clinical	ENSP00000269217.5:p.Pro126=
NM_000227.4:c.378A=	NP_000218.3:p.Pro126=
NM_000227.5:c.378A=	NP_000218.3:p.Pro126=
NM_001127717.2:c.5205A=	NP_001121189.2:p.Pro1735=
NM_001127717.3:c.5205A=	NP_001121189.2:p.Pro1735=
NM_001127717.4:c.5205A=	NP_001121189.2:p.Pro1735=
NM_001127718.2:c.378A=	NP_001121190.2:p.Pro126=
NM_001127718.3:c.378A=	NP_001121190.2:p.Pro126=
NM_001127718.4:c.378A=	NP_001121190.2:p.Pro126=
NM_198129.2:c.5205A=	NP_937762.2:p.Pro1735=
NM_198129.3:c.5205A=	NP_937762.2:p.Pro1735=
ENST00000269217.10:c.378A=	ENSP00000269217.5:p.Pro126=
ENST00000313654.13:c.5205A=	ENSP00000324532.8:p.Pro1735=
ENST00000399516.7:c.5205A=	ENSP00000382432.2:p.Pro1735=
ENST00000587184.5:c.378A=	ENSP00000466557.1:p.Pro126=
ENST00000649721.1:c.2097A=	ENSP00000497885.1:p.Pro699=
XM_011525978.1:c.5232A=	XP_011524280.1:p.Pro1744=
XM_011525978.2:c.5232A=	XP_011524280.1:p.Pro1744=
XM_011525979.1:c.5223A=	XP_011524281.1:p.Pro1741=
XM_011525979.2:c.5223A=	XP_011524281.1:p.Pro1741=
XM_011525980.1:c.5214A=	XP_011524282.1:p.Pro1738=
XM_011525980.2:c.5214A=	XP_011524282.1:p.Pro1738=
XM_011525981.1:c.5100A=	XP_011524283.1:p.Pro1700=
XM_011525981.2:c.5100A=	XP_011524283.1:p.Pro1700=
XM_011525982.1:c.5232A=	XP_011524284.1:p.Pro1744=
XM_011525982.2:c.5232A=	XP_011524284.1:p.Pro1744=
XM_017025743.1:c.3084A=	XP_016881232.1:p.Pro1028=
XM_017025744.1:c.774A=	XP_016881233.1:p.Pro258=
XR_001753199.1:n.5473A=