Canonical Allele Identifier: CA2683557409
Gene: SEMA3E HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83407125del , CM000669.2:g.83407125del GRCh38
NC_000007.13:g.83036441del , CM000669.1:g.83036441del GRCh37
NC_000007.12:g.82874377del NCBI36
NG_021242.1:g.247041del
NG_021242.2:g.247041del

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.607del ENSP00000405052.1:p.Tyr203ThrfsTer9
ENST00000642232.1:c.787del ENSP00000494064.1:p.Tyr263ThrfsTer9
ENST00000643230.2:c.787del MANE Select ENSP00000496491.1:p.Tyr263ThrfsTer9
ENST00000643441.1:n.772del
ENST00000307792.7:c.787del ENSP00000303212.3:p.Tyr263ThrfsTer9
ENST00000427262.5:c.607del ENSP00000405052.1:p.Tyr203ThrfsTer9
NM_001178129.1:c.607del NP_001171600.1:p.Tyr203ThrfsTer9
NM_012431.2:c.787del NP_036563.1:p.Tyr263ThrfsTer9
XM_011516715.1:c.787del XP_011515017.1:p.Tyr263ThrfsTer9
NM_012431.3:c.787del MANE Select NP_036563.1:p.Tyr263ThrfsTer9
NM_001178129.2:c.607del NP_001171600.1:p.Tyr203ThrfsTer9