Canonical Allele Identifier: CA1732870655

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107931467T= , CM000669.2:g.107931467T= GRCh38
NC_000007.13:g.107571912T= , CM000669.1:g.107571912T= GRCh37
NC_000007.12:g.107359148T= NCBI36
NG_023255.1:g.76893A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222399.11:c.4426A= (LAMB1) MANE Select ENSP00000222399.6:p.Lys1476=
ENST00000393561.6:c.4015A= (LAMB1) ENSP00000377191.2:p.Lys1339=
ENST00000468518.2:n.2660A= (LAMB1)
ENST00000468999.2:n.2574A= (LAMB1)
ENST00000474380.2:n.1241A= (LAMB1)
ENST00000676574.1:c.*342A= (LAMB1) ENSP00000503081.1:n.*342A=
ENST00000676744.1:n.272A= (LAMB1)
ENST00000676777.1:c.4426A= (LAMB1) ENSP00000504756.1:p.Lys1476=
ENST00000677101.1:c.*4062A= (LAMB1) ENSP00000503156.1:n.*4062A=
ENST00000677144.1:c.*1245A= (LAMB1) ENSP00000503049.1:n.*1245A=
ENST00000677485.1:n.5650A= (LAMB1)
ENST00000677588.1:c.*657A= (LAMB1) ENSP00000502938.1:n.*657A=
ENST00000677793.1:c.4114A= (LAMB1) ENSP00000504020.1:p.Lys1372=
ENST00000677801.1:c.*255A= (LAMB1) ENSP00000503438.1:n.*255A=
ENST00000678232.1:n.4615A= (LAMB1)
ENST00000678310.1:n.2595A= (LAMB1)
ENST00000678698.1:c.*498A= (LAMB1) ENSP00000503198.1:n.*498A=
ENST00000678704.1:c.*3008A= (LAMB1) ENSP00000504589.1:n.*3008A=
ENST00000678892.1:c.*498A= (LAMB1) ENSP00000504841.1:n.*498A=
ENST00000679200.1:c.*498A= (LAMB1) ENSP00000503498.1:n.*498A=
ENST00000222399.10:c.4426A= (LAMB1) ENSP00000222399.6:p.Lys1476=
ENST00000393561.5:c.4498A= (LAMB1) ENSP00000377191.1:p.Lys1500=
ENST00000417551.5:c.*161T= (DLD) ENSP00000390667.1:n.*161T=
ENST00000468518.1:n.485A= (LAMB1)
ENST00000474380.1:n.663A= (LAMB1)
NM_002291.2:c.4426A= (LAMB1) NP_002282.2:p.Lys1476=
XM_017012201.1:c.4498A= (LAMB1) XP_016867690.1:p.Lys1500=
XR_001744756.1:n.5345A= (LAMB1)
NM_002291.3:c.4426A= (LAMB1) MANE Select NP_002282.2:p.Lys1476=