Canonical Allele Identifier: CA2290312364

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23876402_23876403delinsTG , CM000680.2:g.23876402_23876403delinsTG	GRCh38
NC_000018.9:g.21456366_21456367delinsTG , CM000680.1:g.21456366_21456367delinsTG	GRCh37
NC_000018.8:g.19710364_19710365delinsTG	NCBI36
NG_007853.2:g.191805_191806delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.280_281delinsTG MANE Plus Clinical	ENSP00000269217.5:p.Cys94=
ENST00000313654.14:c.5107_5108delinsTG MANE Select	ENSP00000324532.8:p.Cys1703=
ENST00000649721.1:c.1999_2000delinsTG	ENSP00000497885.1:p.Cys667=
ENST00000269217.10:c.280_281delinsTG	ENSP00000269217.5:p.Cys94=
ENST00000313654.13:c.5107_5108delinsTG	ENSP00000324532.8:p.Cys1703=
ENST00000399516.7:c.5107_5108delinsTG	ENSP00000382432.2:p.Cys1703=
ENST00000587184.5:c.280_281delinsTG	ENSP00000466557.1:p.Cys94=
NM_000227.4:c.280_281delinsTG	NP_000218.3:p.Cys94=
NM_001127717.2:c.5107_5108delinsTG	NP_001121189.2:p.Cys1703=
NM_001127718.2:c.280_281delinsTG	NP_001121190.2:p.Cys94=
NM_198129.2:c.5107_5108delinsTG	NP_937762.2:p.Cys1703=
XM_011525978.1:c.5134_5135delinsTG	XP_011524280.1:p.Cys1712=
XM_011525979.1:c.5125_5126delinsTG	XP_011524281.1:p.Cys1709=
XM_011525980.1:c.5116_5117delinsTG	XP_011524282.1:p.Cys1706=
XM_011525981.1:c.5002_5003delinsTG	XP_011524283.1:p.Cys1668=
XM_011525982.1:c.5134_5135delinsTG	XP_011524284.1:p.Cys1712=
XM_011525978.2:c.5134_5135delinsTG	XP_011524280.1:p.Cys1712=
XM_011525979.2:c.5125_5126delinsTG	XP_011524281.1:p.Cys1709=
XM_011525980.2:c.5116_5117delinsTG	XP_011524282.1:p.Cys1706=
XM_011525981.2:c.5002_5003delinsTG	XP_011524283.1:p.Cys1668=
XM_011525982.2:c.5134_5135delinsTG	XP_011524284.1:p.Cys1712=
XM_017025743.1:c.2986_2987delinsTG	XP_016881232.1:p.Cys996=
XM_017025744.1:c.676_677delinsTG	XP_016881233.1:p.Cys226=
XR_001753199.1:n.5375_5376delinsTG
NM_000227.5:c.280_281delinsTG	NP_000218.3:p.Cys94=
NM_001127717.3:c.5107_5108delinsTG	NP_001121189.2:p.Cys1703=
NM_001127718.3:c.280_281delinsTG	NP_001121190.2:p.Cys94=
NM_198129.3:c.5107_5108delinsTG	NP_937762.2:p.Cys1703=
NM_000227.6:c.280_281delinsTG MANE Plus Clinical	NP_000218.3:p.Cys94=
NM_001127717.4:c.5107_5108delinsTG	NP_001121189.2:p.Cys1703=
NM_001127718.4:c.280_281delinsTG	NP_001121190.2:p.Cys94=
NM_198129.4:c.5107_5108delinsTG MANE Select	NP_937762.2:p.Cys1703=