Canonical Allele Identifier: CA2290323939

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23903042G= , CM000680.2:g.23903042G=	GRCh38
NC_000018.9:g.21483006G= , CM000680.1:g.21483006G=	GRCh37
NC_000018.8:g.19737004G=	NCBI36
NG_007853.2:g.218445G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1408G= MANE Plus Clinical	ENSP00000269217.5:p.Asp470=
ENST00000313654.14:c.6235G= MANE Select	ENSP00000324532.8:p.Asp2079=
ENST00000649721.1:c.3127G=	ENSP00000497885.1:p.Asp1043=
ENST00000269217.10:c.1408G=	ENSP00000269217.5:p.Asp470=
ENST00000313654.13:c.6235G=	ENSP00000324532.8:p.Asp2079=
ENST00000399516.7:c.6067G=	ENSP00000382432.2:p.Asp2023=
ENST00000586751.5:c.1013G=
ENST00000587184.5:c.1240G=	ENSP00000466557.1:p.Asp414=
ENST00000588770.5:n.813G=
NM_000227.4:c.1408G=	NP_000218.3:p.Asp470=
NM_001127717.2:c.6067G=	NP_001121189.2:p.Asp2023=
NM_001127718.2:c.1240G=	NP_001121190.2:p.Asp414=
NM_198129.2:c.6235G=	NP_937762.2:p.Asp2079=
XM_011525978.1:c.6262G=	XP_011524280.1:p.Asp2088=
XM_011525979.1:c.6253G=	XP_011524281.1:p.Asp2085=
XM_011525980.1:c.6244G=	XP_011524282.1:p.Asp2082=
XM_011525981.1:c.6130G=	XP_011524283.1:p.Asp2044=
XM_011525982.1:c.6262G=	XP_011524284.1:p.Asp2088=
XM_011525978.2:c.6262G=	XP_011524280.1:p.Asp2088=
XM_011525979.2:c.6253G=	XP_011524281.1:p.Asp2085=
XM_011525980.2:c.6244G=	XP_011524282.1:p.Asp2082=
XM_011525981.2:c.6130G=	XP_011524283.1:p.Asp2044=
XM_011525982.2:c.6262G=	XP_011524284.1:p.Asp2088=
XM_017025743.1:c.4114G=	XP_016881232.1:p.Asp1372=
XM_017025744.1:c.1804G=	XP_016881233.1:p.Asp602=
XR_001753199.1:n.6503G=
NM_000227.5:c.1408G=	NP_000218.3:p.Asp470=
NM_001127717.3:c.6067G=	NP_001121189.2:p.Asp2023=
NM_001127718.3:c.1240G=	NP_001121190.2:p.Asp414=
NM_198129.3:c.6235G=	NP_937762.2:p.Asp2079=
NM_000227.6:c.1408G= MANE Plus Clinical	NP_000218.3:p.Asp470=
NM_001127717.4:c.6067G=	NP_001121189.2:p.Asp2023=
NM_001127718.4:c.1240G=	NP_001121190.2:p.Asp414=
NM_198129.4:c.6235G= MANE Select	NP_937762.2:p.Asp2079=