Canonical Allele Identifier: CA368863901

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107931394A>C , CM000669.2:g.107931394A>C GRCh38
NC_000007.13:g.107571839A>C , CM000669.1:g.107571839A>C GRCh37
NC_000007.12:g.107359075A>C NCBI36
NG_023255.1:g.76966T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222399.11:c.4499T>G (LAMB1) MANE Select ENSP00000222399.6:p.Leu1500Arg
ENST00000393561.6:c.4088T>G (LAMB1) ENSP00000377191.2:p.Leu1363Arg
ENST00000468518.2:n.2733T>G (LAMB1)
ENST00000468999.2:n.2647T>G (LAMB1)
ENST00000474380.2:n.1314T>G (LAMB1)
ENST00000676574.1:c.*415T>G (LAMB1) ENSP00000503081.1:n.*415T>G
ENST00000676744.1:n.345T>G (LAMB1)
ENST00000676777.1:c.4499T>G (LAMB1) ENSP00000504756.1:p.Leu1500Arg
ENST00000677101.1:c.*4135T>G (LAMB1) ENSP00000503156.1:n.*4135T>G
ENST00000677144.1:c.*1318T>G (LAMB1) ENSP00000503049.1:n.*1318T>G
ENST00000677485.1:n.5723T>G (LAMB1)
ENST00000677588.1:c.*730T>G (LAMB1) ENSP00000502938.1:n.*730T>G
ENST00000677793.1:c.4187T>G (LAMB1) ENSP00000504020.1:p.Leu1396Arg
ENST00000677801.1:c.*328T>G (LAMB1) ENSP00000503438.1:n.*328T>G
ENST00000677883.1:n.10T>G (LAMB1)
ENST00000678232.1:n.4688T>G (LAMB1)
ENST00000678310.1:n.2668T>G (LAMB1)
ENST00000678698.1:c.*571T>G (LAMB1) ENSP00000503198.1:n.*571T>G
ENST00000678704.1:c.*3081T>G (LAMB1) ENSP00000504589.1:n.*3081T>G
ENST00000678892.1:c.*571T>G (LAMB1) ENSP00000504841.1:n.*571T>G
ENST00000679200.1:c.*571T>G (LAMB1) ENSP00000503498.1:n.*571T>G
ENST00000222399.10:c.4499T>G (LAMB1) ENSP00000222399.6:p.Leu1500Arg
ENST00000393561.5:c.4571T>G (LAMB1) ENSP00000377191.1:p.Leu1524Arg
ENST00000417551.5:c.*125-37A>C (DLD) ENSP00000390667.1:n.*125-37A>C
ENST00000468518.1:n.558T>G (LAMB1)
ENST00000474380.1:n.736T>G (LAMB1)
NM_002291.2:c.4499T>G (LAMB1) NP_002282.2:p.Leu1500Arg
XM_017012201.1:c.4571T>G (LAMB1) XP_016867690.1:p.Leu1524Arg
XR_001744756.1:n.5418T>G (LAMB1)
NM_002291.3:c.4499T>G (LAMB1) MANE Select NP_002282.2:p.Leu1500Arg