Canonical Allele Identifier: CA1721679637
Gene: SEMA3E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83407420A= , CM000669.2:g.83407420A= GRCh38
NC_000007.13:g.83036736A= , CM000669.1:g.83036736A= GRCh37
NC_000007.12:g.82874672A= NCBI36
NG_021242.1:g.246744T=
NG_021242.2:g.246744T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.491-181T= ENSP00000405052.1:n.491-181T=
ENST00000642232.1:c.671-181T= ENSP00000494064.1:n.671-181T=
ENST00000643230.2:c.671-181T= MANE Select ENSP00000496491.1:n.671-181T=
ENST00000643441.1:n.656-181T=
ENST00000644381.1:n.234-181T=
ENST00000307792.7:c.671-181T= ENSP00000303212.3:n.671-181T=
ENST00000427262.5:c.491-181T= ENSP00000405052.1:n.491-181T=
NM_001178129.1:c.491-181T= NP_001171600.1:n.491-181T=
NM_012431.2:c.671-181T= NP_036563.1:n.671-181T=
XM_011516715.1:c.671-181T= XP_011515017.1:n.671-181T=
NM_012431.3:c.671-181T= MANE Select NP_036563.1:n.671-181T=
NM_001178129.2:c.491-181T= NP_001171600.1:n.491-181T=