Canonical Allele Identifier: CA2290326009

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23907863A= , CM000680.2:g.23907863A=	GRCh38
NC_000018.9:g.21487827A= , CM000680.1:g.21487827A=	GRCh37
NC_000018.8:g.19741825A=	NCBI36
NG_007853.2:g.223266A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2116A= MANE Plus Clinical	ENSP00000269217.5:p.Arg706=
ENST00000313654.14:c.6943A= MANE Select	ENSP00000324532.8:p.Arg2315=
ENST00000649721.1:c.3611-1290A=	ENSP00000497885.1:n.3611-1290A=
ENST00000269217.10:c.2116A=	ENSP00000269217.5:p.Arg706=
ENST00000313654.13:c.6943A=	ENSP00000324532.8:p.Arg2315=
ENST00000399516.7:c.6775A=	ENSP00000382432.2:p.Arg2259=
ENST00000586751.5:c.1721A=
ENST00000587184.5:c.1948A=	ENSP00000466557.1:p.Arg650=
ENST00000588770.5:n.1521A=
NM_000227.4:c.2116A=	NP_000218.3:p.Arg706=
NM_001127717.2:c.6775A=	NP_001121189.2:p.Arg2259=
NM_001127718.2:c.1948A=	NP_001121190.2:p.Arg650=
NM_198129.2:c.6943A=	NP_937762.2:p.Arg2315=
XM_011525978.1:c.6970A=	XP_011524280.1:p.Arg2324=
XM_011525979.1:c.6961A=	XP_011524281.1:p.Arg2321=
XM_011525980.1:c.6952A=	XP_011524282.1:p.Arg2318=
XM_011525981.1:c.6838A=	XP_011524283.1:p.Arg2280=
XM_011525982.1:c.6746-1290A=	XP_011524284.1:n.6746-1290A=
XM_011525978.2:c.6970A=	XP_011524280.1:p.Arg2324=
XM_011525979.2:c.6961A=	XP_011524281.1:p.Arg2321=
XM_011525980.2:c.6952A=	XP_011524282.1:p.Arg2318=
XM_011525981.2:c.6838A=	XP_011524283.1:p.Arg2280=
XM_011525982.2:c.6746-1290A=	XP_011524284.1:n.6746-1290A=
XM_017025743.1:c.4822A=	XP_016881232.1:p.Arg1608=
XM_017025744.1:c.2512A=	XP_016881233.1:p.Arg838=
XR_001753199.1:n.7211A=
NM_000227.5:c.2116A=	NP_000218.3:p.Arg706=
NM_001127717.3:c.6775A=	NP_001121189.2:p.Arg2259=
NM_001127718.3:c.1948A=	NP_001121190.2:p.Arg650=
NM_198129.3:c.6943A=	NP_937762.2:p.Arg2315=
NM_000227.6:c.2116A= MANE Plus Clinical	NP_000218.3:p.Arg706=
NM_001127717.4:c.6775A=	NP_001121189.2:p.Arg2259=
NM_001127718.4:c.1948A=	NP_001121190.2:p.Arg650=
NM_198129.4:c.6943A= MANE Select	NP_937762.2:p.Arg2315=