Canonical Allele Identifier: CA2290310977
Gene: LAMA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23873068A= , CM000680.2:g.23873068A= GRCh38
NC_000018.9:g.21453032A= , CM000680.1:g.21453032A= GRCh37
NC_000018.8:g.19707030A= NCBI36
NG_007853.2:g.188471A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269217.11:c.24A= MANE Plus Clinical ENSP00000269217.5:p.Ser8=
ENST00000313654.14:c.4998+1407A= MANE Select ENSP00000324532.8:n.4998+1407A=
ENST00000649721.1:c.1890+1407A= ENSP00000497885.1:n.1890+1407A=
ENST00000269217.10:c.24A= ENSP00000269217.5:p.Ser8=
ENST00000313654.13:c.4998+1407A= ENSP00000324532.8:n.4998+1407A=
ENST00000399516.7:c.4998+1407A= ENSP00000382432.2:n.4998+1407A=
ENST00000587184.5:c.24A= ENSP00000466557.1:p.Ser8=
NM_000227.4:c.24A= NP_000218.3:p.Ser8=
NM_001127717.2:c.4998+1407A= NP_001121189.2:n.4998+1407A=
NM_001127718.2:c.24A= NP_001121190.2:p.Ser8=
NM_198129.2:c.4998+1407A= NP_937762.2:n.4998+1407A=
XM_011525978.1:c.5025+1407A= XP_011524280.1:n.5025+1407A=
XM_011525979.1:c.5016+1407A= XP_011524281.1:n.5016+1407A=
XM_011525980.1:c.5007+1407A= XP_011524282.1:n.5007+1407A=
XM_011525981.1:c.4893+1407A= XP_011524283.1:n.4893+1407A=
XM_011525982.1:c.5025+1407A= XP_011524284.1:n.5025+1407A=
XM_011525978.2:c.5025+1407A= XP_011524280.1:n.5025+1407A=
XM_011525979.2:c.5016+1407A= XP_011524281.1:n.5016+1407A=
XM_011525980.2:c.5007+1407A= XP_011524282.1:n.5007+1407A=
XM_011525981.2:c.4893+1407A= XP_011524283.1:n.4893+1407A=
XM_011525982.2:c.5025+1407A= XP_011524284.1:n.5025+1407A=
XM_017025743.1:c.2877+1407A= XP_016881232.1:n.2877+1407A=
XM_017025744.1:c.567+1407A= XP_016881233.1:n.567+1407A=
XR_001753199.1:n.5266+1407A=
NM_000227.5:c.24A= NP_000218.3:p.Ser8=
NM_001127717.3:c.4998+1407A= NP_001121189.2:n.4998+1407A=
NM_001127718.3:c.24A= NP_001121190.2:p.Ser8=
NM_198129.3:c.4998+1407A= NP_937762.2:n.4998+1407A=
NM_000227.6:c.24A= MANE Plus Clinical NP_000218.3:p.Ser8=
NM_001127717.4:c.4998+1407A= NP_001121189.2:n.4998+1407A=
NM_001127718.4:c.24A= NP_001121190.2:p.Ser8=
NM_198129.4:c.4998+1407A= MANE Select NP_937762.2:n.4998+1407A=