Canonical Allele Identifier: CA1732870523

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107931378C= , CM000669.2:g.107931378C= GRCh38
NC_000007.13:g.107571823C= , CM000669.1:g.107571823C= GRCh37
NC_000007.12:g.107359059C= NCBI36
NG_023255.1:g.76982G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222399.11:c.4515G= (LAMB1) MANE Select ENSP00000222399.6:p.Lys1505=
ENST00000393561.6:c.4104G= (LAMB1) ENSP00000377191.2:p.Lys1368=
ENST00000468518.2:n.2749G= (LAMB1)
ENST00000468999.2:n.2663G= (LAMB1)
ENST00000474380.2:n.1330G= (LAMB1)
ENST00000676574.1:c.*431G= (LAMB1) ENSP00000503081.1:n.*431G=
ENST00000676744.1:n.361G= (LAMB1)
ENST00000676777.1:c.4515G= (LAMB1) ENSP00000504756.1:p.Lys1505=
ENST00000677101.1:c.*4151G= (LAMB1) ENSP00000503156.1:n.*4151G=
ENST00000677144.1:c.*1334G= (LAMB1) ENSP00000503049.1:n.*1334G=
ENST00000677485.1:n.5739G= (LAMB1)
ENST00000677588.1:c.*746G= (LAMB1) ENSP00000502938.1:n.*746G=
ENST00000677793.1:c.4203G= (LAMB1) ENSP00000504020.1:p.Lys1401=
ENST00000677801.1:c.*344G= (LAMB1) ENSP00000503438.1:n.*344G=
ENST00000677883.1:n.26G= (LAMB1)
ENST00000678232.1:n.4704G= (LAMB1)
ENST00000678310.1:n.2684G= (LAMB1)
ENST00000678698.1:c.*587G= (LAMB1) ENSP00000503198.1:n.*587G=
ENST00000678704.1:c.*3097G= (LAMB1) ENSP00000504589.1:n.*3097G=
ENST00000678892.1:c.*587G= (LAMB1) ENSP00000504841.1:n.*587G=
ENST00000679200.1:c.*587G= (LAMB1) ENSP00000503498.1:n.*587G=
ENST00000222399.10:c.4515G= (LAMB1) ENSP00000222399.6:p.Lys1505=
ENST00000393561.5:c.4587G= (LAMB1) ENSP00000377191.1:p.Lys1529=
ENST00000417551.5:c.*125-53C= (DLD) ENSP00000390667.1:n.*125-53C=
ENST00000468518.1:n.574G= (LAMB1)
ENST00000474380.1:n.752G= (LAMB1)
NM_002291.2:c.4515G= (LAMB1) NP_002282.2:p.Lys1505=
XM_017012201.1:c.4587G= (LAMB1) XP_016867690.1:p.Lys1529=
XR_001744756.1:n.5434G= (LAMB1)
NM_002291.3:c.4515G= (LAMB1) MANE Select NP_002282.2:p.Lys1505=