Canonical Allele Identifier: CA1721662214
Gene: SEMA3E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83392844A= , CM000669.2:g.83392844A= GRCh38
NC_000007.13:g.83022160A= , CM000669.1:g.83022160A= GRCh37
NC_000007.12:g.82860096A= NCBI36
NG_021242.1:g.261320T=
NG_021242.2:g.261320T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.1321-123T= ENSP00000405052.1:n.1321-123T=
ENST00000642232.1:c.1501-123T= ENSP00000494064.1:n.1501-123T=
ENST00000643230.2:c.1501-123T= MANE Select ENSP00000496491.1:n.1501-123T=
ENST00000643441.1:n.1486-123T=
ENST00000307792.7:c.1501-123T= ENSP00000303212.3:n.1501-123T=
ENST00000427262.5:c.1321-123T= ENSP00000405052.1:n.1321-123T=
NM_001178129.1:c.1321-123T= NP_001171600.1:n.1321-123T=
NM_012431.2:c.1501-123T= NP_036563.1:n.1501-123T=
XM_011516715.1:c.1501-123T= XP_011515017.1:n.1501-123T=
NM_012431.3:c.1501-123T= MANE Select NP_036563.1:n.1501-123T=
NM_001178129.2:c.1321-123T= NP_001171600.1:n.1321-123T=