Canonical Allele Identifier: CA2290325057

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23905581A= , CM000680.2:g.23905581A=	GRCh38
NC_000018.9:g.21485545A= , CM000680.1:g.21485545A=	GRCh37
NC_000018.8:g.19739543A=	NCBI36
NG_007853.2:g.220984A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1848A= MANE Plus Clinical	ENSP00000269217.5:p.Lys616=
ENST00000313654.14:c.6675A= MANE Select	ENSP00000324532.8:p.Lys2225=
ENST00000649721.1:c.3567A=	ENSP00000497885.1:p.Lys1189=
ENST00000269217.10:c.1848A=	ENSP00000269217.5:p.Lys616=
ENST00000313654.13:c.6675A=	ENSP00000324532.8:p.Lys2225=
ENST00000399516.7:c.6507A=	ENSP00000382432.2:p.Lys2169=
ENST00000586751.5:c.1453A=
ENST00000587184.5:c.1680A=	ENSP00000466557.1:p.Lys560=
ENST00000588770.5:n.1253A=
NM_000227.4:c.1848A=	NP_000218.3:p.Lys616=
NM_001127717.2:c.6507A=	NP_001121189.2:p.Lys2169=
NM_001127718.2:c.1680A=	NP_001121190.2:p.Lys560=
NM_198129.2:c.6675A=	NP_937762.2:p.Lys2225=
XM_011525978.1:c.6702A=	XP_011524280.1:p.Lys2234=
XM_011525979.1:c.6693A=	XP_011524281.1:p.Lys2231=
XM_011525980.1:c.6684A=	XP_011524282.1:p.Lys2228=
XM_011525981.1:c.6570A=	XP_011524283.1:p.Lys2190=
XM_011525982.1:c.6702A=	XP_011524284.1:p.Lys2234=
XM_011525978.2:c.6702A=	XP_011524280.1:p.Lys2234=
XM_011525979.2:c.6693A=	XP_011524281.1:p.Lys2231=
XM_011525980.2:c.6684A=	XP_011524282.1:p.Lys2228=
XM_011525981.2:c.6570A=	XP_011524283.1:p.Lys2190=
XM_011525982.2:c.6702A=	XP_011524284.1:p.Lys2234=
XM_017025743.1:c.4554A=	XP_016881232.1:p.Lys1518=
XM_017025744.1:c.2244A=	XP_016881233.1:p.Lys748=
XR_001753199.1:n.6943A=
NM_000227.5:c.1848A=	NP_000218.3:p.Lys616=
NM_001127717.3:c.6507A=	NP_001121189.2:p.Lys2169=
NM_001127718.3:c.1680A=	NP_001121190.2:p.Lys560=
NM_198129.3:c.6675A=	NP_937762.2:p.Lys2225=
NM_000227.6:c.1848A= MANE Plus Clinical	NP_000218.3:p.Lys616=
NM_001127717.4:c.6507A=	NP_001121189.2:p.Lys2169=
NM_001127718.4:c.1680A=	NP_001121190.2:p.Lys560=
NM_198129.4:c.6675A= MANE Select	NP_937762.2:p.Lys2225=