Canonical Allele Identifier: CA1732870609

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107931433T= , CM000669.2:g.107931433T= GRCh38
NC_000007.13:g.107571878T= , CM000669.1:g.107571878T= GRCh37
NC_000007.12:g.107359114T= NCBI36
NG_023255.1:g.76927A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222399.11:c.4460A= (LAMB1) MANE Select ENSP00000222399.6:p.Asn1487=
ENST00000393561.6:c.4049A= (LAMB1) ENSP00000377191.2:p.Asn1350=
ENST00000468518.2:n.2694A= (LAMB1)
ENST00000468999.2:n.2608A= (LAMB1)
ENST00000474380.2:n.1275A= (LAMB1)
ENST00000676574.1:c.*376A= (LAMB1) ENSP00000503081.1:n.*376A=
ENST00000676744.1:n.306A= (LAMB1)
ENST00000676777.1:c.4460A= (LAMB1) ENSP00000504756.1:p.Asn1487=
ENST00000677101.1:c.*4096A= (LAMB1) ENSP00000503156.1:n.*4096A=
ENST00000677144.1:c.*1279A= (LAMB1) ENSP00000503049.1:n.*1279A=
ENST00000677485.1:n.5684A= (LAMB1)
ENST00000677588.1:c.*691A= (LAMB1) ENSP00000502938.1:n.*691A=
ENST00000677793.1:c.4148A= (LAMB1) ENSP00000504020.1:p.Asn1383=
ENST00000677801.1:c.*289A= (LAMB1) ENSP00000503438.1:n.*289A=
ENST00000678232.1:n.4649A= (LAMB1)
ENST00000678310.1:n.2629A= (LAMB1)
ENST00000678698.1:c.*532A= (LAMB1) ENSP00000503198.1:n.*532A=
ENST00000678704.1:c.*3042A= (LAMB1) ENSP00000504589.1:n.*3042A=
ENST00000678892.1:c.*532A= (LAMB1) ENSP00000504841.1:n.*532A=
ENST00000679200.1:c.*532A= (LAMB1) ENSP00000503498.1:n.*532A=
ENST00000222399.10:c.4460A= (LAMB1) ENSP00000222399.6:p.Asn1487=
ENST00000393561.5:c.4532A= (LAMB1) ENSP00000377191.1:p.Asn1511=
ENST00000417551.5:c.*127T= (DLD) ENSP00000390667.1:n.*127T=
ENST00000468518.1:n.519A= (LAMB1)
ENST00000474380.1:n.697A= (LAMB1)
NM_002291.2:c.4460A= (LAMB1) NP_002282.2:p.Asn1487=
XM_017012201.1:c.4532A= (LAMB1) XP_016867690.1:p.Asn1511=
XR_001744756.1:n.5379A= (LAMB1)
NM_002291.3:c.4460A= (LAMB1) MANE Select NP_002282.2:p.Asn1487=