Canonical Allele Identifier: CA2776732712

Gene: SEMA3E

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83407175_83407176insCCAAACACACCCAACACA , CM000669.2:g.83407175_83407176insCCAAACACACCCAACACA	GRCh38
NC_000007.13:g.83036491_83036492insCCAAACACACCCAACACA , CM000669.1:g.83036491_83036492insCCAAACACACCCAACACA	GRCh37
NC_000007.12:g.82874427_82874428insCCAAACACACCCAACACA	NCBI36
NG_021242.1:g.246989_246990insGTGTTGGGTGTGTTTGGT
NG_021242.2:g.246989_246990insGTGTTGGGTGTGTTTGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.555_556insGTGTTGGGTGTGTTTGGT	ENSP00000405052.1:p.Tyr185_Phe186insValLeuGlyValPheGly
ENST00000642232.1:c.735_736insGTGTTGGGTGTGTTTGGT	ENSP00000494064.1:p.Tyr245_Phe246insValLeuGlyValPheGly
ENST00000643230.2:c.735_736insGTGTTGGGTGTGTTTGGT MANE Select	ENSP00000496491.1:p.Tyr245_Phe246insValLeuGlyValPheGly
ENST00000643441.1:n.720_721insGTGTTGGGTGTGTTTGGT
ENST00000644381.1:n.298_299insGTGTTGGGTGTGTTTGGT
ENST00000307792.7:c.735_736insGTGTTGGGTGTGTTTGGT	ENSP00000303212.3:p.Tyr245_Phe246insValLeuGlyValPheGly
ENST00000427262.5:c.555_556insGTGTTGGGTGTGTTTGGT	ENSP00000405052.1:p.Tyr185_Phe186insValLeuGlyValPheGly
NM_001178129.1:c.555_556insGTGTTGGGTGTGTTTGGT	NP_001171600.1:p.Tyr185_Phe186insValLeuGlyValPheGly
NM_012431.2:c.735_736insGTGTTGGGTGTGTTTGGT	NP_036563.1:p.Tyr245_Phe246insValLeuGlyValPheGly
XM_011516715.1:c.735_736insGTGTTGGGTGTGTTTGGT	XP_011515017.1:p.Tyr245_Phe246insValLeuGlyValPheGly
NM_012431.3:c.735_736insGTGTTGGGTGTGTTTGGT MANE Select	NP_036563.1:p.Tyr245_Phe246insValLeuGlyValPheGly
NM_001178129.2:c.555_556insGTGTTGGGTGTGTTTGGT	NP_001171600.1:p.Tyr185_Phe186insValLeuGlyValPheGly