Canonical Allele Identifier: CA164268555

Linked Data

dbSNP Id: rs148159658

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107931399C>T , CM000669.2:g.107931399C>T GRCh38
NC_000007.13:g.107571844C>T , CM000669.1:g.107571844C>T GRCh37
NC_000007.12:g.107359080C>T NCBI36
NG_023255.1:g.76961G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222399.11:c.4494G>A (LAMB1) MANE Select ENSP00000222399.6:p.Glu1498=
ENST00000393561.6:c.4083G>A (LAMB1) ENSP00000377191.2:p.Glu1361=
ENST00000468518.2:n.2728G>A (LAMB1)
ENST00000468999.2:n.2642G>A (LAMB1)
ENST00000474380.2:n.1309G>A (LAMB1)
ENST00000676574.1:c.*410G>A (LAMB1) ENSP00000503081.1:n.*410G>A
ENST00000676744.1:n.340G>A (LAMB1)
ENST00000676777.1:c.4494G>A (LAMB1) ENSP00000504756.1:p.Glu1498=
ENST00000677101.1:c.*4130G>A (LAMB1) ENSP00000503156.1:n.*4130G>A
ENST00000677144.1:c.*1313G>A (LAMB1) ENSP00000503049.1:n.*1313G>A
ENST00000677485.1:n.5718G>A (LAMB1)
ENST00000677588.1:c.*725G>A (LAMB1) ENSP00000502938.1:n.*725G>A
ENST00000677793.1:c.4182G>A (LAMB1) ENSP00000504020.1:p.Glu1394=
ENST00000677801.1:c.*323G>A (LAMB1) ENSP00000503438.1:n.*323G>A
ENST00000677883.1:n.5G>A (LAMB1)
ENST00000678232.1:n.4683G>A (LAMB1)
ENST00000678310.1:n.2663G>A (LAMB1)
ENST00000678698.1:c.*566G>A (LAMB1) ENSP00000503198.1:n.*566G>A
ENST00000678704.1:c.*3076G>A (LAMB1) ENSP00000504589.1:n.*3076G>A
ENST00000678892.1:c.*566G>A (LAMB1) ENSP00000504841.1:n.*566G>A
ENST00000679200.1:c.*566G>A (LAMB1) ENSP00000503498.1:n.*566G>A
ENST00000222399.10:c.4494G>A (LAMB1) ENSP00000222399.6:p.Glu1498=
ENST00000393561.5:c.4566G>A (LAMB1) ENSP00000377191.1:p.Glu1522=
ENST00000417551.5:c.*125-32C>T (DLD) ENSP00000390667.1:n.*125-32C>T
ENST00000468518.1:n.553G>A (LAMB1)
ENST00000474380.1:n.731G>A (LAMB1)
NM_002291.2:c.4494G>A (LAMB1) NP_002282.2:p.Glu1498=
XM_017012201.1:c.4566G>A (LAMB1) XP_016867690.1:p.Glu1522=
XR_001744756.1:n.5413G>A (LAMB1)
NM_002291.3:c.4494G>A (LAMB1) MANE Select NP_002282.2:p.Glu1498=