Canonical Allele Identifier: CA2290322189

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23898822C= , CM000680.2:g.23898822C=	GRCh38
NC_000018.9:g.21478786C= , CM000680.1:g.21478786C=	GRCh37
NC_000018.8:g.19732784C=	NCBI36
NG_007853.2:g.214225C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.871C= MANE Plus Clinical	ENSP00000269217.5:p.Gln291=
ENST00000313654.14:c.5698C= MANE Select	ENSP00000324532.8:p.Gln1900=
ENST00000649721.1:c.2590C=	ENSP00000497885.1:p.Gln864=
ENST00000269217.10:c.871C=	ENSP00000269217.5:p.Gln291=
ENST00000313654.13:c.5698C=	ENSP00000324532.8:p.Gln1900=
ENST00000399516.7:c.5698C=	ENSP00000382432.2:p.Gln1900=
ENST00000586709.1:n.86C=
ENST00000586751.5:c.476C=
ENST00000587184.5:c.871C=	ENSP00000466557.1:p.Gln291=
ENST00000588770.5:n.276C=
NM_000227.4:c.871C=	NP_000218.3:p.Gln291=
NM_001127717.2:c.5698C=	NP_001121189.2:p.Gln1900=
NM_001127718.2:c.871C=	NP_001121190.2:p.Gln291=
NM_198129.2:c.5698C=	NP_937762.2:p.Gln1900=
XM_011525978.1:c.5725C=	XP_011524280.1:p.Gln1909=
XM_011525979.1:c.5716C=	XP_011524281.1:p.Gln1906=
XM_011525980.1:c.5707C=	XP_011524282.1:p.Gln1903=
XM_011525981.1:c.5593C=	XP_011524283.1:p.Gln1865=
XM_011525982.1:c.5725C=	XP_011524284.1:p.Gln1909=
XM_011525978.2:c.5725C=	XP_011524280.1:p.Gln1909=
XM_011525979.2:c.5716C=	XP_011524281.1:p.Gln1906=
XM_011525980.2:c.5707C=	XP_011524282.1:p.Gln1903=
XM_011525981.2:c.5593C=	XP_011524283.1:p.Gln1865=
XM_011525982.2:c.5725C=	XP_011524284.1:p.Gln1909=
XM_017025743.1:c.3577C=	XP_016881232.1:p.Gln1193=
XM_017025744.1:c.1267C=	XP_016881233.1:p.Gln423=
XR_001753199.1:n.5966C=
NM_000227.5:c.871C=	NP_000218.3:p.Gln291=
NM_001127717.3:c.5698C=	NP_001121189.2:p.Gln1900=
NM_001127718.3:c.871C=	NP_001121190.2:p.Gln291=
NM_198129.3:c.5698C=	NP_937762.2:p.Gln1900=
NM_000227.6:c.871C= MANE Plus Clinical	NP_000218.3:p.Gln291=
NM_001127717.4:c.5698C=	NP_001121189.2:p.Gln1900=
NM_001127718.4:c.871C=	NP_001121190.2:p.Gln291=
NM_198129.4:c.5698C= MANE Select	NP_937762.2:p.Gln1900=