Canonical Allele Identifier: CA1721679481

Gene: SEMA3E

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83407074_83407077delinsCATA , CM000669.2:g.83407074_83407077delinsCATA	GRCh38
NC_000007.13:g.83036390_83036393delinsCATA , CM000669.1:g.83036390_83036393delinsCATA	GRCh37
NC_000007.12:g.82874326_82874329delinsCATA	NCBI36
NG_021242.1:g.247087_247090delinsTATG
NG_021242.2:g.247087_247090delinsTATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.633+20_633+23delinsTATG	ENSP00000405052.1:n.633+20_633+23delinsTATG
ENST00000642232.1:c.813+20_813+23delinsTATG	ENSP00000494064.1:n.813+20_813+23delinsTATG
ENST00000643230.2:c.813+20_813+23delinsTATG MANE Select	ENSP00000496491.1:n.813+20_813+23delinsTATG
ENST00000643441.1:n.798+20_798+23delinsTATG
ENST00000307792.7:c.813+20_813+23delinsTATG	ENSP00000303212.3:n.813+20_813+23delinsTATG
ENST00000427262.5:c.633+20_633+23delinsTATG	ENSP00000405052.1:n.633+20_633+23delinsTATG
NM_001178129.1:c.633+20_633+23delinsTATG	NP_001171600.1:n.633+20_633+23delinsTATG
NM_012431.2:c.813+20_813+23delinsTATG	NP_036563.1:n.813+20_813+23delinsTATG
XM_011516715.1:c.813+20_813+23delinsTATG	XP_011515017.1:n.813+20_813+23delinsTATG
NM_012431.3:c.813+20_813+23delinsTATG MANE Select	NP_036563.1:n.813+20_813+23delinsTATG
NM_001178129.2:c.633+20_633+23delinsTATG	NP_001171600.1:n.633+20_633+23delinsTATG