Canonical Allele Identifier: CA2776732309
Gene: SEMA3E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83392602_83392622del , CM000669.2:g.83392602_83392622del GRCh38
NC_000007.13:g.83021918_83021938del , CM000669.1:g.83021918_83021938del GRCh37
NC_000007.12:g.82859854_82859874del NCBI36
NG_021242.1:g.261543_261563del
NG_021242.2:g.261543_261563del

Transcript Alleles

HGVS Amino-acid change
ENST00000427262.6:c.1421_1441del ENSP00000405052.1:p.Asp474_Asp480del
ENST00000642232.1:c.1601_1621del ENSP00000494064.1:p.Asp534_Asp540del
ENST00000643230.2:c.1601_1621del MANE Select ENSP00000496491.1:p.Asp534_Asp540del
ENST00000643441.1:n.1586_1606del
ENST00000307792.7:c.1601_1621del ENSP00000303212.3:p.Asp534_Asp540del
ENST00000427262.5:c.1421_1441del ENSP00000405052.1:p.Asp474_Asp480del
NM_001178129.1:c.1421_1441del NP_001171600.1:p.Asp474_Asp480del
NM_012431.2:c.1601_1621del NP_036563.1:p.Asp534_Asp540del
XM_011516715.1:c.1601_1621del XP_011515017.1:p.Asp534_Asp540del
NM_012431.3:c.1601_1621del MANE Select NP_036563.1:p.Asp534_Asp540del
NM_001178129.2:c.1421_1441del NP_001171600.1:p.Asp474_Asp480del