Canonical Allele Identifier: CA1732869615
Gene: LAMB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107951546_107951550delinsATTAT , CM000669.2:g.107951546_107951550delinsATTAT GRCh38
NC_000007.13:g.107591991_107591995delinsATTAT , CM000669.1:g.107591991_107591995delinsATTAT GRCh37
NC_000007.12:g.107379227_107379231delinsATTAT NCBI36
NG_023255.1:g.56810_56814delinsATAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000222399.11:c.3295-228_3295-224delinsATAAT MANE Select ENSP00000222399.6:n.3295-228_3295-224delinsATAAT
ENST00000393561.6:c.2884-228_2884-224delinsATAAT ENSP00000377191.2:n.2884-228_2884-224delinsATAAT
ENST00000676574.1:c.3295-228_3295-224delinsATAAT ENSP00000503081.1:n.3295-228_3295-224delinsATAAT
ENST00000676777.1:c.3295-228_3295-224delinsATAAT ENSP00000504756.1:n.3295-228_3295-224delinsATAAT
ENST00000676920.1:c.2884-228_2884-224delinsATAAT ENSP00000503814.1:n.2884-228_2884-224delinsATAAT
ENST00000677101.1:c.*2931-228_*2931-224delinsATAAT ENSP00000503156.1:n.*2931-228_*2931-224delinsATAAT
ENST00000677144.1:c.*114-228_*114-224delinsATAAT ENSP00000503049.1:n.*114-228_*114-224delinsATAAT
ENST00000677485.1:n.4519-228_4519-224delinsATAAT
ENST00000677588.1:c.3295-228_3295-224delinsATAAT ENSP00000502938.1:n.3295-228_3295-224delinsATAAT
ENST00000677652.1:n.3484-228_3484-224delinsATAAT
ENST00000677793.1:c.3079+1980_3079+1984delinsATAAT ENSP00000504020.1:n.3079+1980_3079+1984delinsATAAT
ENST00000677801.1:c.2884-228_2884-224delinsATAAT ENSP00000503438.1:n.2884-228_2884-224delinsATAAT
ENST00000677994.1:n.3461-228_3461-224delinsATAAT
ENST00000678232.1:n.3484-228_3484-224delinsATAAT
ENST00000678266.1:n.3437-228_3437-224delinsATAAT
ENST00000678346.1:c.*2931-228_*2931-224delinsATAAT ENSP00000504349.1:n.*2931-228_*2931-224delinsATAAT
ENST00000678698.1:c.2884-228_2884-224delinsATAAT ENSP00000503198.1:n.2884-228_2884-224delinsATAAT
ENST00000678704.1:c.*1877-228_*1877-224delinsATAAT ENSP00000504589.1:n.*1877-228_*1877-224delinsATAAT
ENST00000678892.1:c.3295-228_3295-224delinsATAAT ENSP00000504841.1:n.3295-228_3295-224delinsATAAT
ENST00000679173.1:n.3484-228_3484-224delinsATAAT
ENST00000679200.1:c.2884-228_2884-224delinsATAAT ENSP00000503498.1:n.2884-228_2884-224delinsATAAT
ENST00000679244.1:c.3295-228_3295-224delinsATAAT ENSP00000504656.1:n.3295-228_3295-224delinsATAAT
ENST00000222399.10:c.3295-228_3295-224delinsATAAT ENSP00000222399.6:n.3295-228_3295-224delinsATAAT
ENST00000393561.5:c.3367-228_3367-224delinsATAAT ENSP00000377191.1:n.3367-228_3367-224delinsATAAT
ENST00000476039.1:n.336-228_336-224delinsATAAT
ENST00000479448.1:n.83-228_83-224delinsATAAT
NM_002291.2:c.3295-228_3295-224delinsATAAT NP_002282.2:n.3295-228_3295-224delinsATAAT
XM_011516203.1:c.3295-228_3295-224delinsATAAT XP_011514505.1:n.3295-228_3295-224delinsATAAT
XM_017012201.1:c.3367-228_3367-224delinsATAAT XP_016867690.1:n.3367-228_3367-224delinsATAAT
XM_017012202.1:c.3367-228_3367-224delinsATAAT XP_016867691.1:n.3367-228_3367-224delinsATAAT
XR_001744756.1:n.4098-228_4098-224delinsATAAT
NM_002291.3:c.3295-228_3295-224delinsATAAT MANE Select NP_002282.2:n.3295-228_3295-224delinsATAAT