Canonical Allele Identifier: CA1721679496
Gene: SEMA3E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83407107C= , CM000669.2:g.83407107C= GRCh38
NC_000007.13:g.83036423C= , CM000669.1:g.83036423C= GRCh37
NC_000007.12:g.82874359C= NCBI36
NG_021242.1:g.247057G=
NG_021242.2:g.247057G=

Transcript Alleles

HGVS Amino-acid change
ENST00000427262.6:c.623G= ENSP00000405052.1:p.Arg208=
ENST00000642232.1:c.803G= ENSP00000494064.1:p.Arg268=
ENST00000643230.2:c.803G= MANE Select ENSP00000496491.1:p.Arg268=
ENST00000643441.1:n.788G=
ENST00000307792.7:c.803G= ENSP00000303212.3:p.Arg268=
ENST00000427262.5:c.623G= ENSP00000405052.1:p.Arg208=
NM_001178129.1:c.623G= NP_001171600.1:p.Arg208=
NM_012431.2:c.803G= NP_036563.1:p.Arg268=
XM_011516715.1:c.803G= XP_011515017.1:p.Arg268=
NM_012431.3:c.803G= MANE Select NP_036563.1:p.Arg268=
NM_001178129.2:c.623G= NP_001171600.1:p.Arg208=