Canonical Allele Identifier: CA368864024

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107931421T>C , CM000669.2:g.107931421T>C GRCh38
NC_000007.13:g.107571866T>C , CM000669.1:g.107571866T>C GRCh37
NC_000007.12:g.107359102T>C NCBI36
NG_023255.1:g.76939A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222399.11:c.4472A>G (LAMB1) MANE Select ENSP00000222399.6:p.Glu1491Gly
ENST00000393561.6:c.4061A>G (LAMB1) ENSP00000377191.2:p.Glu1354Gly
ENST00000468518.2:n.2706A>G (LAMB1)
ENST00000468999.2:n.2620A>G (LAMB1)
ENST00000474380.2:n.1287A>G (LAMB1)
ENST00000676574.1:c.*388A>G (LAMB1) ENSP00000503081.1:n.*388A>G
ENST00000676744.1:n.318A>G (LAMB1)
ENST00000676777.1:c.4472A>G (LAMB1) ENSP00000504756.1:p.Glu1491Gly
ENST00000677101.1:c.*4108A>G (LAMB1) ENSP00000503156.1:n.*4108A>G
ENST00000677144.1:c.*1291A>G (LAMB1) ENSP00000503049.1:n.*1291A>G
ENST00000677485.1:n.5696A>G (LAMB1)
ENST00000677588.1:c.*703A>G (LAMB1) ENSP00000502938.1:n.*703A>G
ENST00000677793.1:c.4160A>G (LAMB1) ENSP00000504020.1:p.Glu1387Gly
ENST00000677801.1:c.*301A>G (LAMB1) ENSP00000503438.1:n.*301A>G
ENST00000678232.1:n.4661A>G (LAMB1)
ENST00000678310.1:n.2641A>G (LAMB1)
ENST00000678698.1:c.*544A>G (LAMB1) ENSP00000503198.1:n.*544A>G
ENST00000678704.1:c.*3054A>G (LAMB1) ENSP00000504589.1:n.*3054A>G
ENST00000678892.1:c.*544A>G (LAMB1) ENSP00000504841.1:n.*544A>G
ENST00000679200.1:c.*544A>G (LAMB1) ENSP00000503498.1:n.*544A>G
ENST00000222399.10:c.4472A>G (LAMB1) ENSP00000222399.6:p.Glu1491Gly
ENST00000393561.5:c.4544A>G (LAMB1) ENSP00000377191.1:p.Glu1515Gly
ENST00000417551.5:c.*125-10T>C (DLD) ENSP00000390667.1:n.*125-10T>C
ENST00000468518.1:n.531A>G (LAMB1)
ENST00000474380.1:n.709A>G (LAMB1)
NM_002291.2:c.4472A>G (LAMB1) NP_002282.2:p.Glu1491Gly
XM_017012201.1:c.4544A>G (LAMB1) XP_016867690.1:p.Glu1515Gly
XR_001744756.1:n.5391A>G (LAMB1)
NM_002291.3:c.4472A>G (LAMB1) MANE Select NP_002282.2:p.Glu1491Gly