Canonical Allele Identifier: CA1732870570

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107931409T= , CM000669.2:g.107931409T= GRCh38
NC_000007.13:g.107571854T= , CM000669.1:g.107571854T= GRCh37
NC_000007.12:g.107359090T= NCBI36
NG_023255.1:g.76951A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222399.11:c.4484A= (LAMB1) MANE Select ENSP00000222399.6:p.Lys1495=
ENST00000393561.6:c.4073A= (LAMB1) ENSP00000377191.2:p.Lys1358=
ENST00000468518.2:n.2718A= (LAMB1)
ENST00000468999.2:n.2632A= (LAMB1)
ENST00000474380.2:n.1299A= (LAMB1)
ENST00000676574.1:c.*400A= (LAMB1) ENSP00000503081.1:n.*400A=
ENST00000676744.1:n.330A= (LAMB1)
ENST00000676777.1:c.4484A= (LAMB1) ENSP00000504756.1:p.Lys1495=
ENST00000677101.1:c.*4120A= (LAMB1) ENSP00000503156.1:n.*4120A=
ENST00000677144.1:c.*1303A= (LAMB1) ENSP00000503049.1:n.*1303A=
ENST00000677485.1:n.5708A= (LAMB1)
ENST00000677588.1:c.*715A= (LAMB1) ENSP00000502938.1:n.*715A=
ENST00000677793.1:c.4172A= (LAMB1) ENSP00000504020.1:p.Lys1391=
ENST00000677801.1:c.*313A= (LAMB1) ENSP00000503438.1:n.*313A=
ENST00000678232.1:n.4673A= (LAMB1)
ENST00000678310.1:n.2653A= (LAMB1)
ENST00000678698.1:c.*556A= (LAMB1) ENSP00000503198.1:n.*556A=
ENST00000678704.1:c.*3066A= (LAMB1) ENSP00000504589.1:n.*3066A=
ENST00000678892.1:c.*556A= (LAMB1) ENSP00000504841.1:n.*556A=
ENST00000679200.1:c.*556A= (LAMB1) ENSP00000503498.1:n.*556A=
ENST00000222399.10:c.4484A= (LAMB1) ENSP00000222399.6:p.Lys1495=
ENST00000393561.5:c.4556A= (LAMB1) ENSP00000377191.1:p.Lys1519=
ENST00000417551.5:c.*125-22T= (DLD) ENSP00000390667.1:n.*125-22T=
ENST00000468518.1:n.543A= (LAMB1)
ENST00000474380.1:n.721A= (LAMB1)
NM_002291.2:c.4484A= (LAMB1) NP_002282.2:p.Lys1495=
XM_017012201.1:c.4556A= (LAMB1) XP_016867690.1:p.Lys1519=
XR_001744756.1:n.5403A= (LAMB1)
NM_002291.3:c.4484A= (LAMB1) MANE Select NP_002282.2:p.Lys1495=