Canonical Allele Identifier: CA368874921
Gene: LAMB1 HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107973011C>T , CM000669.2:g.107973011C>T GRCh38
NC_000007.13:g.107613456C>T , CM000669.1:g.107613456C>T GRCh37
NC_000007.12:g.107400692C>T NCBI36
NG_023255.1:g.35349G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222399.11:c.1543G>A MANE Select ENSP00000222399.6:p.Gly515Arg
ENST00000393561.6:c.1132G>A ENSP00000377191.2:p.Gly378Arg
ENST00000439976.6:c.1801G>A ENSP00000412686.2:p.Gly601Arg
ENST00000676574.1:c.1543G>A ENSP00000503081.1:p.Gly515Arg
ENST00000676777.1:c.1543G>A ENSP00000504756.1:p.Gly515Arg
ENST00000676920.1:c.1132G>A ENSP00000503814.1:p.Gly378Arg
ENST00000677101.1:c.*1179G>A ENSP00000503156.1:n.*1179G>A
ENST00000677144.1:c.1543G>A ENSP00000503049.1:p.Gly515Arg
ENST00000677485.1:n.2767G>A
ENST00000677588.1:c.1543G>A ENSP00000502938.1:p.Gly515Arg
ENST00000677652.1:n.1732G>A
ENST00000677734.1:n.1732G>A
ENST00000677793.1:c.1543G>A ENSP00000504020.1:p.Gly515Arg
ENST00000677801.1:c.1132G>A ENSP00000503438.1:p.Gly378Arg
ENST00000677994.1:n.1709G>A
ENST00000678232.1:n.1732G>A
ENST00000678266.1:n.1685G>A
ENST00000678346.1:c.*1179G>A ENSP00000504349.1:n.*1179G>A
ENST00000678698.1:c.1132G>A ENSP00000503198.1:p.Gly378Arg
ENST00000678704.1:c.*125G>A ENSP00000504589.1:n.*125G>A
ENST00000678892.1:c.1543G>A ENSP00000504841.1:p.Gly515Arg
ENST00000679173.1:n.1732G>A
ENST00000679200.1:c.1132G>A ENSP00000503498.1:p.Gly378Arg
ENST00000679244.1:c.1543G>A ENSP00000504656.1:p.Gly515Arg
ENST00000222399.10:c.1543G>A ENSP00000222399.6:p.Gly515Arg
ENST00000393560.5:c.1543G>A ENSP00000377190.1:p.Gly515Arg
ENST00000393561.5:c.1615G>A ENSP00000377191.1:p.Gly539Arg
NM_002291.2:c.1543G>A NP_002282.2:p.Gly515Arg
XM_011516203.1:c.1543G>A XP_011514505.1:p.Gly515Arg
XM_017012201.1:c.1615G>A XP_016867690.1:p.Gly539Arg
XM_017012202.1:c.1615G>A XP_016867691.1:p.Gly539Arg
XR_001744756.1:n.2346G>A
NM_002291.3:c.1543G>A MANE Select NP_002282.2:p.Gly515Arg