Canonical Allele Identifier: CA1721679518
Gene: SEMA3E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83407162C= , CM000669.2:g.83407162C= GRCh38
NC_000007.13:g.83036478C= , CM000669.1:g.83036478C= GRCh37
NC_000007.12:g.82874414C= NCBI36
NG_021242.1:g.247002G=
NG_021242.2:g.247002G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.568G= ENSP00000405052.1:p.Glu190=
ENST00000642232.1:c.748G= ENSP00000494064.1:p.Glu250=
ENST00000643230.2:c.748G= MANE Select ENSP00000496491.1:p.Glu250=
ENST00000643441.1:n.733G=
ENST00000644381.1:n.311G=
ENST00000307792.7:c.748G= ENSP00000303212.3:p.Glu250=
ENST00000427262.5:c.568G= ENSP00000405052.1:p.Glu190=
NM_001178129.1:c.568G= NP_001171600.1:p.Glu190=
NM_012431.2:c.748G= NP_036563.1:p.Glu250=
XM_011516715.1:c.748G= XP_011515017.1:p.Glu250=
NM_012431.3:c.748G= MANE Select NP_036563.1:p.Glu250=
NM_001178129.2:c.568G= NP_001171600.1:p.Glu190=