Canonical Allele Identifier: CA2683557418
Gene: SEMA3E HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83407255del , CM000669.2:g.83407255del GRCh38
NC_000007.13:g.83036571del , CM000669.1:g.83036571del GRCh37
NC_000007.12:g.82874507del NCBI36
NG_021242.1:g.246914del
NG_021242.2:g.246914del

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.491-11del ENSP00000405052.1:n.491-11del
ENST00000642232.1:c.671-11del ENSP00000494064.1:n.671-11del
ENST00000643230.2:c.671-11del MANE Select ENSP00000496491.1:n.671-11del
ENST00000643441.1:n.656-11del
ENST00000644381.1:n.234-11del
ENST00000307792.7:c.671-11del ENSP00000303212.3:n.671-11del
ENST00000427262.5:c.491-11del ENSP00000405052.1:n.491-11del
NM_001178129.1:c.491-11del NP_001171600.1:n.491-11del
NM_012431.2:c.671-11del NP_036563.1:n.671-11del
XM_011516715.1:c.671-11del XP_011515017.1:n.671-11del
NM_012431.3:c.671-11del MANE Select NP_036563.1:n.671-11del
NM_001178129.2:c.491-11del NP_001171600.1:n.491-11del