Canonical Allele Identifier: CA367930168
Gene: SEMA3E HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83407105G>T , CM000669.2:g.83407105G>T GRCh38
NC_000007.13:g.83036421G>T , CM000669.1:g.83036421G>T GRCh37
NC_000007.12:g.82874357G>T NCBI36
NG_021242.1:g.247059C>A
NG_021242.2:g.247059C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000427262.6:c.625C>A ENSP00000405052.1:p.Leu209Ile
ENST00000642232.1:c.805C>A ENSP00000494064.1:p.Leu269Ile
ENST00000643230.2:c.805C>A MANE Select ENSP00000496491.1:p.Leu269Ile
ENST00000643441.1:n.790C>A
ENST00000307792.7:c.805C>A ENSP00000303212.3:p.Leu269Ile
ENST00000427262.5:c.625C>A ENSP00000405052.1:p.Leu209Ile
NM_001178129.1:c.625C>A NP_001171600.1:p.Leu209Ile
NM_012431.2:c.805C>A NP_036563.1:p.Leu269Ile
XM_011516715.1:c.805C>A XP_011515017.1:p.Leu269Ile
NM_012431.3:c.805C>A MANE Select NP_036563.1:p.Leu269Ile
NM_001178129.2:c.625C>A NP_001171600.1:p.Leu209Ile