Canonical Allele Identifier: CA2290325073

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23905618A= , CM000680.2:g.23905618A=	GRCh38
NC_000018.9:g.21485582A= , CM000680.1:g.21485582A=	GRCh37
NC_000018.8:g.19739580A=	NCBI36
NG_007853.2:g.221021A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.1885A= MANE Plus Clinical	ENSP00000269217.5:p.Lys629=
ENST00000313654.14:c.6712A= MANE Select	ENSP00000324532.8:p.Lys2238=
ENST00000649721.1:c.3604A=	ENSP00000497885.1:p.Lys1202=
ENST00000269217.10:c.1885A=	ENSP00000269217.5:p.Lys629=
ENST00000313654.13:c.6712A=	ENSP00000324532.8:p.Lys2238=
ENST00000399516.7:c.6544A=	ENSP00000382432.2:p.Lys2182=
ENST00000586751.5:c.1490A=
ENST00000587184.5:c.1717A=	ENSP00000466557.1:p.Lys573=
ENST00000588770.5:n.1290A=
NM_000227.4:c.1885A=	NP_000218.3:p.Lys629=
NM_001127717.2:c.6544A=	NP_001121189.2:p.Lys2182=
NM_001127718.2:c.1717A=	NP_001121190.2:p.Lys573=
NM_198129.2:c.6712A=	NP_937762.2:p.Lys2238=
XM_011525978.1:c.6739A=	XP_011524280.1:p.Lys2247=
XM_011525979.1:c.6730A=	XP_011524281.1:p.Lys2244=
XM_011525980.1:c.6721A=	XP_011524282.1:p.Lys2241=
XM_011525981.1:c.6607A=	XP_011524283.1:p.Lys2203=
XM_011525982.1:c.6739A=	XP_011524284.1:p.Lys2247=
XM_011525978.2:c.6739A=	XP_011524280.1:p.Lys2247=
XM_011525979.2:c.6730A=	XP_011524281.1:p.Lys2244=
XM_011525980.2:c.6721A=	XP_011524282.1:p.Lys2241=
XM_011525981.2:c.6607A=	XP_011524283.1:p.Lys2203=
XM_011525982.2:c.6739A=	XP_011524284.1:p.Lys2247=
XM_017025743.1:c.4591A=	XP_016881232.1:p.Lys1531=
XM_017025744.1:c.2281A=	XP_016881233.1:p.Lys761=
XR_001753199.1:n.6980A=
NM_000227.5:c.1885A=	NP_000218.3:p.Lys629=
NM_001127717.3:c.6544A=	NP_001121189.2:p.Lys2182=
NM_001127718.3:c.1717A=	NP_001121190.2:p.Lys573=
NM_198129.3:c.6712A=	NP_937762.2:p.Lys2238=
NM_000227.6:c.1885A= MANE Plus Clinical	NP_000218.3:p.Lys629=
NM_001127717.4:c.6544A=	NP_001121189.2:p.Lys2182=
NM_001127718.4:c.1717A=	NP_001121190.2:p.Lys573=
NM_198129.4:c.6712A= MANE Select	NP_937762.2:p.Lys2238=