Canonical Allele Identifier: CA367930169
Gene: SEMA3E HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000427262.6:c.623G>T ENSP00000405052.1:p.Arg208Leu
ENST00000642232.1:c.803G>T ENSP00000494064.1:p.Arg268Leu
ENST00000643230.2:c.803G>T MANE Select ENSP00000496491.1:p.Arg268Leu
ENST00000643441.1:n.788G>T
ENST00000307792.7:c.803G>T ENSP00000303212.3:p.Arg268Leu
ENST00000427262.5:c.623G>T ENSP00000405052.1:p.Arg208Leu
NM_001178129.1:c.623G>T NP_001171600.1:p.Arg208Leu
NM_012431.2:c.803G>T NP_036563.1:p.Arg268Leu
XM_011516715.1:c.803G>T XP_011515017.1:p.Arg268Leu
NM_012431.3:c.803G>T MANE Select NP_036563.1:p.Arg268Leu
NM_001178129.2:c.623G>T NP_001171600.1:p.Arg208Leu