Canonical Allele Identifier: CA2290323942

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23903046T= , CM000680.2:g.23903046T=	GRCh38
NC_000018.9:g.21483010T= , CM000680.1:g.21483010T=	GRCh37
NC_000018.8:g.19737008T=	NCBI36
NG_007853.2:g.218449T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1412T= MANE Plus Clinical	ENSP00000269217.5:p.Phe471=
ENST00000313654.14:c.6239T= MANE Select	ENSP00000324532.8:p.Phe2080=
ENST00000649721.1:c.3131T=	ENSP00000497885.1:p.Phe1044=
ENST00000269217.10:c.1412T=	ENSP00000269217.5:p.Phe471=
ENST00000313654.13:c.6239T=	ENSP00000324532.8:p.Phe2080=
ENST00000399516.7:c.6071T=	ENSP00000382432.2:p.Phe2024=
ENST00000586751.5:c.1017T=
ENST00000587184.5:c.1244T=	ENSP00000466557.1:p.Phe415=
ENST00000588770.5:n.817T=
NM_000227.4:c.1412T=	NP_000218.3:p.Phe471=
NM_001127717.2:c.6071T=	NP_001121189.2:p.Phe2024=
NM_001127718.2:c.1244T=	NP_001121190.2:p.Phe415=
NM_198129.2:c.6239T=	NP_937762.2:p.Phe2080=
XM_011525978.1:c.6266T=	XP_011524280.1:p.Phe2089=
XM_011525979.1:c.6257T=	XP_011524281.1:p.Phe2086=
XM_011525980.1:c.6248T=	XP_011524282.1:p.Phe2083=
XM_011525981.1:c.6134T=	XP_011524283.1:p.Phe2045=
XM_011525982.1:c.6266T=	XP_011524284.1:p.Phe2089=
XM_011525978.2:c.6266T=	XP_011524280.1:p.Phe2089=
XM_011525979.2:c.6257T=	XP_011524281.1:p.Phe2086=
XM_011525980.2:c.6248T=	XP_011524282.1:p.Phe2083=
XM_011525981.2:c.6134T=	XP_011524283.1:p.Phe2045=
XM_011525982.2:c.6266T=	XP_011524284.1:p.Phe2089=
XM_017025743.1:c.4118T=	XP_016881232.1:p.Phe1373=
XM_017025744.1:c.1808T=	XP_016881233.1:p.Phe603=
XR_001753199.1:n.6507T=
NM_000227.5:c.1412T=	NP_000218.3:p.Phe471=
NM_001127717.3:c.6071T=	NP_001121189.2:p.Phe2024=
NM_001127718.3:c.1244T=	NP_001121190.2:p.Phe415=
NM_198129.3:c.6239T=	NP_937762.2:p.Phe2080=
NM_000227.6:c.1412T= MANE Plus Clinical	NP_000218.3:p.Phe471=
NM_001127717.4:c.6071T=	NP_001121189.2:p.Phe2024=
NM_001127718.4:c.1244T=	NP_001121190.2:p.Phe415=
NM_198129.4:c.6239T= MANE Select	NP_937762.2:p.Phe2080=