Canonical Allele Identifier: CA2684481541
Gene: LAMB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107973105G>C , CM000669.2:g.107973105G>C GRCh38
NC_000007.13:g.107613550G>C , CM000669.1:g.107613550G>C GRCh37
NC_000007.12:g.107400786G>C NCBI36
NG_023255.1:g.35255C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222399.11:c.1483-34C>G MANE Select ENSP00000222399.6:n.1483-34C>G
ENST00000393561.6:c.1072-34C>G ENSP00000377191.2:n.1072-34C>G
ENST00000439976.6:c.1741-34C>G ENSP00000412686.2:n.1741-34C>G
ENST00000676574.1:c.1483-34C>G ENSP00000503081.1:n.1483-34C>G
ENST00000676777.1:c.1483-34C>G ENSP00000504756.1:n.1483-34C>G
ENST00000676920.1:c.1072-34C>G ENSP00000503814.1:n.1072-34C>G
ENST00000677101.1:c.*1119-34C>G ENSP00000503156.1:n.*1119-34C>G
ENST00000677144.1:c.1483-34C>G ENSP00000503049.1:n.1483-34C>G
ENST00000677485.1:n.2707-34C>G
ENST00000677588.1:c.1483-34C>G ENSP00000502938.1:n.1483-34C>G
ENST00000677652.1:n.1672-34C>G
ENST00000677734.1:n.1672-34C>G
ENST00000677793.1:c.1483-34C>G ENSP00000504020.1:n.1483-34C>G
ENST00000677801.1:c.1072-34C>G ENSP00000503438.1:n.1072-34C>G
ENST00000677994.1:n.1649-34C>G
ENST00000678232.1:n.1672-34C>G
ENST00000678266.1:n.1625-34C>G
ENST00000678346.1:c.*1119-34C>G ENSP00000504349.1:n.*1119-34C>G
ENST00000678698.1:c.1072-34C>G ENSP00000503198.1:n.1072-34C>G
ENST00000678704.1:c.*65-34C>G ENSP00000504589.1:n.*65-34C>G
ENST00000678892.1:c.1483-34C>G ENSP00000504841.1:n.1483-34C>G
ENST00000679173.1:n.1672-34C>G
ENST00000679200.1:c.1072-34C>G ENSP00000503498.1:n.1072-34C>G
ENST00000679244.1:c.1483-34C>G ENSP00000504656.1:n.1483-34C>G
ENST00000222399.10:c.1483-34C>G ENSP00000222399.6:n.1483-34C>G
ENST00000393560.5:c.1483-34C>G ENSP00000377190.1:n.1483-34C>G
ENST00000393561.5:c.1555-34C>G ENSP00000377191.1:n.1555-34C>G
NM_002291.2:c.1483-34C>G NP_002282.2:n.1483-34C>G
XM_011516203.1:c.1483-34C>G XP_011514505.1:n.1483-34C>G
XM_017012201.1:c.1555-34C>G XP_016867690.1:n.1555-34C>G
XM_017012202.1:c.1555-34C>G XP_016867691.1:n.1555-34C>G
XR_001744756.1:n.2286-34C>G
NM_002291.3:c.1483-34C>G MANE Select NP_002282.2:n.1483-34C>G