Canonical Allele Identifier: CA1721679503
Gene: SEMA3E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83407119G= , CM000669.2:g.83407119G= GRCh38
NC_000007.13:g.83036435G= , CM000669.1:g.83036435G= GRCh37
NC_000007.12:g.82874371G= NCBI36
NG_021242.1:g.247045C=
NG_021242.2:g.247045C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.611C= ENSP00000405052.1:p.Thr204=
ENST00000642232.1:c.791C= ENSP00000494064.1:p.Thr264=
ENST00000643230.2:c.791C= MANE Select ENSP00000496491.1:p.Thr264=
ENST00000643441.1:n.776C=
ENST00000307792.7:c.791C= ENSP00000303212.3:p.Thr264=
ENST00000427262.5:c.611C= ENSP00000405052.1:p.Thr204=
NM_001178129.1:c.611C= NP_001171600.1:p.Thr204=
NM_012431.2:c.791C= NP_036563.1:p.Thr264=
XM_011516715.1:c.791C= XP_011515017.1:p.Thr264=
NM_012431.3:c.791C= MANE Select NP_036563.1:p.Thr264=
NM_001178129.2:c.611C= NP_001171600.1:p.Thr204=