Canonical Allele Identifier: CA1721661759
Gene: SEMA3E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83392481_83392484delinsGTTA , CM000669.2:g.83392481_83392484delinsGTTA GRCh38
NC_000007.13:g.83021797_83021800delinsGTTA , CM000669.1:g.83021797_83021800delinsGTTA GRCh37
NC_000007.12:g.82859733_82859736delinsGTTA NCBI36
NG_021242.1:g.261680_261683delinsTAAC
NG_021242.2:g.261680_261683delinsTAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.1487+71_1487+74delinsTAAC ENSP00000405052.1:n.1487+71_1487+74delinsTAAC
ENST00000642232.1:c.1667+71_1667+74delinsTAAC ENSP00000494064.1:n.1667+71_1667+74delinsTAAC
ENST00000643230.2:c.1667+71_1667+74delinsTAAC MANE Select ENSP00000496491.1:n.1667+71_1667+74delinsTAAC
ENST00000643441.1:n.1652+71_1652+74delinsTAAC
ENST00000307792.7:c.1667+71_1667+74delinsTAAC ENSP00000303212.3:n.1667+71_1667+74delinsTAAC
ENST00000427262.5:c.1487+71_1487+74delinsTAAC ENSP00000405052.1:n.1487+71_1487+74delinsTAAC
NM_001178129.1:c.1487+71_1487+74delinsTAAC NP_001171600.1:n.1487+71_1487+74delinsTAAC
NM_012431.2:c.1667+71_1667+74delinsTAAC NP_036563.1:n.1667+71_1667+74delinsTAAC
XM_011516715.1:c.1667+71_1667+74delinsTAAC XP_011515017.1:n.1667+71_1667+74delinsTAAC
NM_012431.3:c.1667+71_1667+74delinsTAAC MANE Select NP_036563.1:n.1667+71_1667+74delinsTAAC
NM_001178129.2:c.1487+71_1487+74delinsTAAC NP_001171600.1:n.1487+71_1487+74delinsTAAC