Canonical Allele Identifier: CA1721679548
Gene: SEMA3E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83407221G= , CM000669.2:g.83407221G= GRCh38
NC_000007.13:g.83036537G= , CM000669.1:g.83036537G= GRCh37
NC_000007.12:g.82874473G= NCBI36
NG_021242.1:g.246943C=
NG_021242.2:g.246943C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.509C= ENSP00000405052.1:p.Ser170=
ENST00000642232.1:c.689C= ENSP00000494064.1:p.Ser230=
ENST00000643230.2:c.689C= MANE Select ENSP00000496491.1:p.Ser230=
ENST00000643441.1:n.674C=
ENST00000644381.1:n.252C=
ENST00000307792.7:c.689C= ENSP00000303212.3:p.Ser230=
ENST00000427262.5:c.509C= ENSP00000405052.1:p.Ser170=
NM_001178129.1:c.509C= NP_001171600.1:p.Ser170=
NM_012431.2:c.689C= NP_036563.1:p.Ser230=
XM_011516715.1:c.689C= XP_011515017.1:p.Ser230=
NM_012431.3:c.689C= MANE Select NP_036563.1:p.Ser230=
NM_001178129.2:c.509C= NP_001171600.1:p.Ser170=