Canonical Allele Identifier: CA1721679544

Gene: SEMA3E

Linked Data

• dbSNP Id: rs1788347241

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83407213_83407214insGAC , CM000669.2:g.83407213_83407214insGAC	GRCh38
NC_000007.13:g.83036529_83036530insGAC , CM000669.1:g.83036529_83036530insGAC	GRCh37
NC_000007.12:g.82874465_82874466insGAC	NCBI36
NG_021242.1:g.246950_246951insGTC
NG_021242.2:g.246950_246951insGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.516_517insGTC	ENSP00000405052.1:p.Met172_Ile173insVal
ENST00000642232.1:c.696_697insGTC	ENSP00000494064.1:p.Met232_Ile233insVal
ENST00000643230.2:c.696_697insGTC MANE Select	ENSP00000496491.1:p.Met232_Ile233insVal
ENST00000643441.1:n.681_682insGTC
ENST00000644381.1:n.259_260insGTC
ENST00000307792.7:c.696_697insGTC	ENSP00000303212.3:p.Met232_Ile233insVal
ENST00000427262.5:c.516_517insGTC	ENSP00000405052.1:p.Met172_Ile173insVal
NM_001178129.1:c.516_517insGTC	NP_001171600.1:p.Met172_Ile173insVal
NM_012431.2:c.696_697insGTC	NP_036563.1:p.Met232_Ile233insVal
XM_011516715.1:c.696_697insGTC	XP_011515017.1:p.Met232_Ile233insVal
NM_012431.3:c.696_697insGTC MANE Select	NP_036563.1:p.Met232_Ile233insVal
NM_001178129.2:c.516_517insGTC	NP_001171600.1:p.Met172_Ile173insVal