Canonical Allele Identifier: CA1721679485

Gene: SEMA3E

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83407079_83407081delinsTGA , CM000669.2:g.83407079_83407081delinsTGA	GRCh38
NC_000007.13:g.83036395_83036397delinsTGA , CM000669.1:g.83036395_83036397delinsTGA	GRCh37
NC_000007.12:g.82874331_82874333delinsTGA	NCBI36
NG_021242.1:g.247083_247085delinsTCA
NG_021242.2:g.247083_247085delinsTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.633+16_633+18delinsTCA	ENSP00000405052.1:n.633+16_633+18delinsTCA
ENST00000642232.1:c.813+16_813+18delinsTCA	ENSP00000494064.1:n.813+16_813+18delinsTCA
ENST00000643230.2:c.813+16_813+18delinsTCA MANE Select	ENSP00000496491.1:n.813+16_813+18delinsTCA
ENST00000643441.1:n.798+16_798+18delinsTCA
ENST00000307792.7:c.813+16_813+18delinsTCA	ENSP00000303212.3:n.813+16_813+18delinsTCA
ENST00000427262.5:c.633+16_633+18delinsTCA	ENSP00000405052.1:n.633+16_633+18delinsTCA
NM_001178129.1:c.633+16_633+18delinsTCA	NP_001171600.1:n.633+16_633+18delinsTCA
NM_012431.2:c.813+16_813+18delinsTCA	NP_036563.1:n.813+16_813+18delinsTCA
XM_011516715.1:c.813+16_813+18delinsTCA	XP_011515017.1:n.813+16_813+18delinsTCA
NM_012431.3:c.813+16_813+18delinsTCA MANE Select	NP_036563.1:n.813+16_813+18delinsTCA
NM_001178129.2:c.633+16_633+18delinsTCA	NP_001171600.1:n.633+16_633+18delinsTCA