Canonical Allele Identifier: CA1721679546
Gene: SEMA3E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83407216T= , CM000669.2:g.83407216T= GRCh38
NC_000007.13:g.83036532T= , CM000669.1:g.83036532T= GRCh37
NC_000007.12:g.82874468T= NCBI36
NG_021242.1:g.246948A=
NG_021242.2:g.246948A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.514A= ENSP00000405052.1:p.Met172=
ENST00000642232.1:c.694A= ENSP00000494064.1:p.Met232=
ENST00000643230.2:c.694A= MANE Select ENSP00000496491.1:p.Met232=
ENST00000643441.1:n.679A=
ENST00000644381.1:n.257A=
ENST00000307792.7:c.694A= ENSP00000303212.3:p.Met232=
ENST00000427262.5:c.514A= ENSP00000405052.1:p.Met172=
NM_001178129.1:c.514A= NP_001171600.1:p.Met172=
NM_012431.2:c.694A= NP_036563.1:p.Met232=
XM_011516715.1:c.694A= XP_011515017.1:p.Met232=
NM_012431.3:c.694A= MANE Select NP_036563.1:p.Met232=
NM_001178129.2:c.514A= NP_001171600.1:p.Met172=