Canonical Allele Identifier: CA2683557385
Gene: SEMA3E HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83407043del , CM000669.2:g.83407043del GRCh38
NC_000007.13:g.83036359del , CM000669.1:g.83036359del GRCh37
NC_000007.12:g.82874295del NCBI36
NG_021242.1:g.247123del
NG_021242.2:g.247123del

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.633+56del ENSP00000405052.1:n.633+56del
ENST00000642232.1:c.813+56del ENSP00000494064.1:n.813+56del
ENST00000643230.2:c.813+56del MANE Select ENSP00000496491.1:n.813+56del
ENST00000643441.1:n.798+56del
ENST00000307792.7:c.813+56del ENSP00000303212.3:n.813+56del
ENST00000427262.5:c.633+56del ENSP00000405052.1:n.633+56del
NM_001178129.1:c.633+56del NP_001171600.1:n.633+56del
NM_012431.2:c.813+56del NP_036563.1:n.813+56del
XM_011516715.1:c.813+56del XP_011515017.1:n.813+56del
NM_012431.3:c.813+56del MANE Select NP_036563.1:n.813+56del
NM_001178129.2:c.633+56del NP_001171600.1:n.633+56del