Canonical Allele Identifier: CA1721679513
Gene: SEMA3E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83407153G= , CM000669.2:g.83407153G= GRCh38
NC_000007.13:g.83036469G= , CM000669.1:g.83036469G= GRCh37
NC_000007.12:g.82874405G= NCBI36
NG_021242.1:g.247011C=
NG_021242.2:g.247011C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.577C= ENSP00000405052.1:p.Leu193=
ENST00000642232.1:c.757C= ENSP00000494064.1:p.Leu253=
ENST00000643230.2:c.757C= MANE Select ENSP00000496491.1:p.Leu253=
ENST00000643441.1:n.742C=
ENST00000644381.1:n.320C=
ENST00000307792.7:c.757C= ENSP00000303212.3:p.Leu253=
ENST00000427262.5:c.577C= ENSP00000405052.1:p.Leu193=
NM_001178129.1:c.577C= NP_001171600.1:p.Leu193=
NM_012431.2:c.757C= NP_036563.1:p.Leu253=
XM_011516715.1:c.757C= XP_011515017.1:p.Leu253=
NM_012431.3:c.757C= MANE Select NP_036563.1:p.Leu253=
NM_001178129.2:c.577C= NP_001171600.1:p.Leu193=