Canonical Allele Identifier: CA1721679542
Gene: SEMA3E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83407212A= , CM000669.2:g.83407212A= GRCh38
NC_000007.13:g.83036528A= , CM000669.1:g.83036528A= GRCh37
NC_000007.12:g.82874464A= NCBI36
NG_021242.1:g.246952T=
NG_021242.2:g.246952T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.518T= ENSP00000405052.1:p.Ile173=
ENST00000642232.1:c.698T= ENSP00000494064.1:p.Ile233=
ENST00000643230.2:c.698T= MANE Select ENSP00000496491.1:p.Ile233=
ENST00000643441.1:n.683T=
ENST00000644381.1:n.261T=
ENST00000307792.7:c.698T= ENSP00000303212.3:p.Ile233=
ENST00000427262.5:c.518T= ENSP00000405052.1:p.Ile173=
NM_001178129.1:c.518T= NP_001171600.1:p.Ile173=
NM_012431.2:c.698T= NP_036563.1:p.Ile233=
XM_011516715.1:c.698T= XP_011515017.1:p.Ile233=
NM_012431.3:c.698T= MANE Select NP_036563.1:p.Ile233=
NM_001178129.2:c.518T= NP_001171600.1:p.Ile173=