Canonical Allele Identifier: CA1732870594

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107931419T= , CM000669.2:g.107931419T= GRCh38
NC_000007.13:g.107571864T= , CM000669.1:g.107571864T= GRCh37
NC_000007.12:g.107359100T= NCBI36
NG_023255.1:g.76941A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222399.11:c.4474A= (LAMB1) MANE Select ENSP00000222399.6:p.Lys1492=
ENST00000393561.6:c.4063A= (LAMB1) ENSP00000377191.2:p.Lys1355=
ENST00000468518.2:n.2708A= (LAMB1)
ENST00000468999.2:n.2622A= (LAMB1)
ENST00000474380.2:n.1289A= (LAMB1)
ENST00000676574.1:c.*390A= (LAMB1) ENSP00000503081.1:n.*390A=
ENST00000676744.1:n.320A= (LAMB1)
ENST00000676777.1:c.4474A= (LAMB1) ENSP00000504756.1:p.Lys1492=
ENST00000677101.1:c.*4110A= (LAMB1) ENSP00000503156.1:n.*4110A=
ENST00000677144.1:c.*1293A= (LAMB1) ENSP00000503049.1:n.*1293A=
ENST00000677485.1:n.5698A= (LAMB1)
ENST00000677588.1:c.*705A= (LAMB1) ENSP00000502938.1:n.*705A=
ENST00000677793.1:c.4162A= (LAMB1) ENSP00000504020.1:p.Lys1388=
ENST00000677801.1:c.*303A= (LAMB1) ENSP00000503438.1:n.*303A=
ENST00000678232.1:n.4663A= (LAMB1)
ENST00000678310.1:n.2643A= (LAMB1)
ENST00000678698.1:c.*546A= (LAMB1) ENSP00000503198.1:n.*546A=
ENST00000678704.1:c.*3056A= (LAMB1) ENSP00000504589.1:n.*3056A=
ENST00000678892.1:c.*546A= (LAMB1) ENSP00000504841.1:n.*546A=
ENST00000679200.1:c.*546A= (LAMB1) ENSP00000503498.1:n.*546A=
ENST00000222399.10:c.4474A= (LAMB1) ENSP00000222399.6:p.Lys1492=
ENST00000393561.5:c.4546A= (LAMB1) ENSP00000377191.1:p.Lys1516=
ENST00000417551.5:c.*125-12T= (DLD) ENSP00000390667.1:n.*125-12T=
ENST00000468518.1:n.533A= (LAMB1)
ENST00000474380.1:n.711A= (LAMB1)
NM_002291.2:c.4474A= (LAMB1) NP_002282.2:p.Lys1492=
XM_017012201.1:c.4546A= (LAMB1) XP_016867690.1:p.Lys1516=
XR_001744756.1:n.5393A= (LAMB1)
NM_002291.3:c.4474A= (LAMB1) MANE Select NP_002282.2:p.Lys1492=