Canonical Allele Identifier: CA1721661963
Gene: SEMA3E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83392622C= , CM000669.2:g.83392622C= GRCh38
NC_000007.13:g.83021938C= , CM000669.1:g.83021938C= GRCh37
NC_000007.12:g.82859874C= NCBI36
NG_021242.1:g.261542G=
NG_021242.2:g.261542G=

Transcript Alleles

HGVS Amino-acid change
ENST00000427262.6:c.1420G= ENSP00000405052.1:p.Asp474=
ENST00000642232.1:c.1600G= ENSP00000494064.1:p.Asp534=
ENST00000643230.2:c.1600G= MANE Select ENSP00000496491.1:p.Asp534=
ENST00000643441.1:n.1585G=
ENST00000307792.7:c.1600G= ENSP00000303212.3:p.Asp534=
ENST00000427262.5:c.1420G= ENSP00000405052.1:p.Asp474=
NM_001178129.1:c.1420G= NP_001171600.1:p.Asp474=
NM_012431.2:c.1600G= NP_036563.1:p.Asp534=
XM_011516715.1:c.1600G= XP_011515017.1:p.Asp534=
NM_012431.3:c.1600G= MANE Select NP_036563.1:p.Asp534=
NM_001178129.2:c.1420G= NP_001171600.1:p.Asp474=