Canonical Allele Identifier: CA1721661757
Gene: SEMA3E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83392480_83392483delinsAGTT , CM000669.2:g.83392480_83392483delinsAGTT GRCh38
NC_000007.13:g.83021796_83021799delinsAGTT , CM000669.1:g.83021796_83021799delinsAGTT GRCh37
NC_000007.12:g.82859732_82859735delinsAGTT NCBI36
NG_021242.1:g.261681_261684delinsAACT
NG_021242.2:g.261681_261684delinsAACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.1487+72_1487+75delinsAACT ENSP00000405052.1:n.1487+72_1487+75delinsAACT
ENST00000642232.1:c.1667+72_1667+75delinsAACT ENSP00000494064.1:n.1667+72_1667+75delinsAACT
ENST00000643230.2:c.1667+72_1667+75delinsAACT MANE Select ENSP00000496491.1:n.1667+72_1667+75delinsAACT
ENST00000643441.1:n.1652+72_1652+75delinsAACT
ENST00000307792.7:c.1667+72_1667+75delinsAACT ENSP00000303212.3:n.1667+72_1667+75delinsAACT
ENST00000427262.5:c.1487+72_1487+75delinsAACT ENSP00000405052.1:n.1487+72_1487+75delinsAACT
NM_001178129.1:c.1487+72_1487+75delinsAACT NP_001171600.1:n.1487+72_1487+75delinsAACT
NM_012431.2:c.1667+72_1667+75delinsAACT NP_036563.1:n.1667+72_1667+75delinsAACT
XM_011516715.1:c.1667+72_1667+75delinsAACT XP_011515017.1:n.1667+72_1667+75delinsAACT
NM_012431.3:c.1667+72_1667+75delinsAACT MANE Select NP_036563.1:n.1667+72_1667+75delinsAACT
NM_001178129.2:c.1487+72_1487+75delinsAACT NP_001171600.1:n.1487+72_1487+75delinsAACT