Canonical Allele Identifier: CA367930465
Gene: SEMA3E HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83407239T>A , CM000669.2:g.83407239T>A GRCh38
NC_000007.13:g.83036555T>A , CM000669.1:g.83036555T>A GRCh37
NC_000007.12:g.82874491T>A NCBI36
NG_021242.1:g.246925A>T
NG_021242.2:g.246925A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.491A>T ENSP00000405052.1:p.Glu164Val
ENST00000642232.1:c.671A>T ENSP00000494064.1:p.Glu224Val
ENST00000643230.2:c.671A>T MANE Select ENSP00000496491.1:p.Glu224Val
ENST00000643441.1:n.656A>T
ENST00000644381.1:n.234A>T
ENST00000307792.7:c.671A>T ENSP00000303212.3:p.Glu224Val
ENST00000427262.5:c.491A>T ENSP00000405052.1:p.Glu164Val
NM_001178129.1:c.491A>T NP_001171600.1:p.Glu164Val
NM_012431.2:c.671A>T NP_036563.1:p.Glu224Val
XM_011516715.1:c.671A>T XP_011515017.1:p.Glu224Val
NM_012431.3:c.671A>T MANE Select NP_036563.1:p.Glu224Val
NM_001178129.2:c.491A>T NP_001171600.1:p.Glu164Val