Canonical Allele Identifier: CA367930334
Gene: SEMA3E HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83407183T>A , CM000669.2:g.83407183T>A GRCh38
NC_000007.13:g.83036499T>A , CM000669.1:g.83036499T>A GRCh37
NC_000007.12:g.82874435T>A NCBI36
NG_021242.1:g.246981A>T
NG_021242.2:g.246981A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.547A>T ENSP00000405052.1:p.Lys183Ter
ENST00000642232.1:c.727A>T ENSP00000494064.1:p.Lys243Ter
ENST00000643230.2:c.727A>T MANE Select ENSP00000496491.1:p.Lys243Ter
ENST00000643441.1:n.712A>T
ENST00000644381.1:n.290A>T
ENST00000307792.7:c.727A>T ENSP00000303212.3:p.Lys243Ter
ENST00000427262.5:c.547A>T ENSP00000405052.1:p.Lys183Ter
NM_001178129.1:c.547A>T NP_001171600.1:p.Lys183Ter
NM_012431.2:c.727A>T NP_036563.1:p.Lys243Ter
XM_011516715.1:c.727A>T XP_011515017.1:p.Lys243Ter
NM_012431.3:c.727A>T MANE Select NP_036563.1:p.Lys243Ter
NM_001178129.2:c.547A>T NP_001171600.1:p.Lys183Ter