Canonical Allele Identifier: CA368863863

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107931385A>C , CM000669.2:g.107931385A>C GRCh38
NC_000007.13:g.107571830A>C , CM000669.1:g.107571830A>C GRCh37
NC_000007.12:g.107359066A>C NCBI36
NG_023255.1:g.76975T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222399.11:c.4508T>G (LAMB1) MANE Select ENSP00000222399.6:p.Leu1503Arg
ENST00000393561.6:c.4097T>G (LAMB1) ENSP00000377191.2:p.Leu1366Arg
ENST00000468518.2:n.2742T>G (LAMB1)
ENST00000468999.2:n.2656T>G (LAMB1)
ENST00000474380.2:n.1323T>G (LAMB1)
ENST00000676574.1:c.*424T>G (LAMB1) ENSP00000503081.1:n.*424T>G
ENST00000676744.1:n.354T>G (LAMB1)
ENST00000676777.1:c.4508T>G (LAMB1) ENSP00000504756.1:p.Leu1503Arg
ENST00000677101.1:c.*4144T>G (LAMB1) ENSP00000503156.1:n.*4144T>G
ENST00000677144.1:c.*1327T>G (LAMB1) ENSP00000503049.1:n.*1327T>G
ENST00000677485.1:n.5732T>G (LAMB1)
ENST00000677588.1:c.*739T>G (LAMB1) ENSP00000502938.1:n.*739T>G
ENST00000677793.1:c.4196T>G (LAMB1) ENSP00000504020.1:p.Leu1399Arg
ENST00000677801.1:c.*337T>G (LAMB1) ENSP00000503438.1:n.*337T>G
ENST00000677883.1:n.19T>G (LAMB1)
ENST00000678232.1:n.4697T>G (LAMB1)
ENST00000678310.1:n.2677T>G (LAMB1)
ENST00000678698.1:c.*580T>G (LAMB1) ENSP00000503198.1:n.*580T>G
ENST00000678704.1:c.*3090T>G (LAMB1) ENSP00000504589.1:n.*3090T>G
ENST00000678892.1:c.*580T>G (LAMB1) ENSP00000504841.1:n.*580T>G
ENST00000679200.1:c.*580T>G (LAMB1) ENSP00000503498.1:n.*580T>G
ENST00000222399.10:c.4508T>G (LAMB1) ENSP00000222399.6:p.Leu1503Arg
ENST00000393561.5:c.4580T>G (LAMB1) ENSP00000377191.1:p.Leu1527Arg
ENST00000417551.5:c.*125-46A>C (DLD) ENSP00000390667.1:n.*125-46A>C
ENST00000468518.1:n.567T>G (LAMB1)
ENST00000474380.1:n.745T>G (LAMB1)
NM_002291.2:c.4508T>G (LAMB1) NP_002282.2:p.Leu1503Arg
XM_017012201.1:c.4580T>G (LAMB1) XP_016867690.1:p.Leu1527Arg
XR_001744756.1:n.5427T>G (LAMB1)
NM_002291.3:c.4508T>G (LAMB1) MANE Select NP_002282.2:p.Leu1503Arg