Canonical Allele Identifier: CA2535062621

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107931541C>A , CM000669.2:g.107931541C>A GRCh38
NC_000007.13:g.107571986C>A , CM000669.1:g.107571986C>A GRCh37
NC_000007.12:g.107359222C>A NCBI36
NG_023255.1:g.76819G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222399.11:c.4393-41G>T (LAMB1) MANE Select ENSP00000222399.6:n.4393-41G>T
ENST00000393561.6:c.3982-41G>T (LAMB1) ENSP00000377191.2:n.3982-41G>T
ENST00000468518.2:n.2627-41G>T (LAMB1)
ENST00000468999.2:n.2541-41G>T (LAMB1)
ENST00000474380.2:n.1208-41G>T (LAMB1)
ENST00000676574.1:c.*309-41G>T (LAMB1) ENSP00000503081.1:n.*309-41G>T
ENST00000676744.1:n.198G>T (LAMB1)
ENST00000676777.1:c.4393-41G>T (LAMB1) ENSP00000504756.1:n.4393-41G>T
ENST00000677101.1:c.*4029-41G>T (LAMB1) ENSP00000503156.1:n.*4029-41G>T
ENST00000677144.1:c.*1212-41G>T (LAMB1) ENSP00000503049.1:n.*1212-41G>T
ENST00000677485.1:n.5617-41G>T (LAMB1)
ENST00000677588.1:c.*624-41G>T (LAMB1) ENSP00000502938.1:n.*624-41G>T
ENST00000677793.1:c.4081-41G>T (LAMB1) ENSP00000504020.1:n.4081-41G>T
ENST00000677801.1:c.*222-41G>T (LAMB1) ENSP00000503438.1:n.*222-41G>T
ENST00000678232.1:n.4582-41G>T (LAMB1)
ENST00000678310.1:n.2562-41G>T (LAMB1)
ENST00000678698.1:c.*465-41G>T (LAMB1) ENSP00000503198.1:n.*465-41G>T
ENST00000678704.1:c.*2975-41G>T (LAMB1) ENSP00000504589.1:n.*2975-41G>T
ENST00000678892.1:c.*465-41G>T (LAMB1) ENSP00000504841.1:n.*465-41G>T
ENST00000679200.1:c.*465-41G>T (LAMB1) ENSP00000503498.1:n.*465-41G>T
ENST00000222399.10:c.4393-41G>T (LAMB1) ENSP00000222399.6:n.4393-41G>T
ENST00000393561.5:c.4465-41G>T (LAMB1) ENSP00000377191.1:n.4465-41G>T
ENST00000417551.5:c.*235C>A (DLD) ENSP00000390667.1:n.*235C>A
ENST00000468518.1:n.452-41G>T (LAMB1)
ENST00000474380.1:n.630-41G>T (LAMB1)
NM_002291.2:c.4393-41G>T (LAMB1) NP_002282.2:n.4393-41G>T
XM_017012201.1:c.4465-41G>T (LAMB1) XP_016867690.1:n.4465-41G>T
XR_001744756.1:n.5312-41G>T (LAMB1)
NM_002291.3:c.4393-41G>T (LAMB1) MANE Select NP_002282.2:n.4393-41G>T