Canonical Allele Identifier: CA2684479179
Gene: LAMB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107951373_107951374insC , CM000669.2:g.107951373_107951374insC GRCh38
NC_000007.13:g.107591818_107591819insC , CM000669.1:g.107591818_107591819insC GRCh37
NC_000007.12:g.107379054_107379055insC NCBI36
NG_023255.1:g.56986_56987insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000222399.11:c.3295-52_3295-51insG MANE Select ENSP00000222399.6:n.3295-52_3295-51insG
ENST00000393561.6:c.2884-52_2884-51insG ENSP00000377191.2:n.2884-52_2884-51insG
ENST00000676574.1:c.3295-52_3295-51insG ENSP00000503081.1:n.3295-52_3295-51insG
ENST00000676777.1:c.3295-52_3295-51insG ENSP00000504756.1:n.3295-52_3295-51insG
ENST00000676920.1:c.2884-52_2884-51insG ENSP00000503814.1:n.2884-52_2884-51insG
ENST00000677101.1:c.*2931-52_*2931-51insG ENSP00000503156.1:n.*2931-52_*2931-51insG
ENST00000677144.1:c.*114-52_*114-51insG ENSP00000503049.1:n.*114-52_*114-51insG
ENST00000677485.1:n.4519-52_4519-51insG
ENST00000677588.1:c.3295-52_3295-51insG ENSP00000502938.1:n.3295-52_3295-51insG
ENST00000677652.1:n.3484-52_3484-51insG
ENST00000677793.1:c.3079+2156_3079+2157insG ENSP00000504020.1:n.3079+2156_3079+2157insG
ENST00000677801.1:c.2884-52_2884-51insG ENSP00000503438.1:n.2884-52_2884-51insG
ENST00000677994.1:n.3461-52_3461-51insG
ENST00000678232.1:n.3484-52_3484-51insG
ENST00000678266.1:n.3437-52_3437-51insG
ENST00000678346.1:c.*2931-52_*2931-51insG ENSP00000504349.1:n.*2931-52_*2931-51insG
ENST00000678698.1:c.2884-52_2884-51insG ENSP00000503198.1:n.2884-52_2884-51insG
ENST00000678704.1:c.*1877-52_*1877-51insG ENSP00000504589.1:n.*1877-52_*1877-51insG
ENST00000678892.1:c.3295-52_3295-51insG ENSP00000504841.1:n.3295-52_3295-51insG
ENST00000679173.1:n.3484-52_3484-51insG
ENST00000679200.1:c.2884-52_2884-51insG ENSP00000503498.1:n.2884-52_2884-51insG
ENST00000679244.1:c.3295-52_3295-51insG ENSP00000504656.1:n.3295-52_3295-51insG
ENST00000222399.10:c.3295-52_3295-51insG ENSP00000222399.6:n.3295-52_3295-51insG
ENST00000393561.5:c.3367-52_3367-51insG ENSP00000377191.1:n.3367-52_3367-51insG
ENST00000476039.1:n.336-52_336-51insG
ENST00000479448.1:n.83-52_83-51insG
NM_002291.2:c.3295-52_3295-51insG NP_002282.2:n.3295-52_3295-51insG
XM_011516203.1:c.3295-52_3295-51insG XP_011514505.1:n.3295-52_3295-51insG
XM_017012201.1:c.3367-52_3367-51insG XP_016867690.1:n.3367-52_3367-51insG
XM_017012202.1:c.3367-52_3367-51insG XP_016867691.1:n.3367-52_3367-51insG
XR_001744756.1:n.4098-52_4098-51insG
NM_002291.3:c.3295-52_3295-51insG MANE Select NP_002282.2:n.3295-52_3295-51insG