Canonical Allele Identifier: CA1721679668
Gene: SEMA3E HGNC NCBI

Linked Data

dbSNP Id: rs1788352586

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83407484del , CM000669.2:g.83407484del GRCh38
NC_000007.13:g.83036800del , CM000669.1:g.83036800del GRCh37
NC_000007.12:g.82874736del NCBI36
NG_021242.1:g.246681del
NG_021242.2:g.246681del

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.491-244del ENSP00000405052.1:n.491-244del
ENST00000642232.1:c.671-244del ENSP00000494064.1:n.671-244del
ENST00000643230.2:c.671-244del MANE Select ENSP00000496491.1:n.671-244del
ENST00000643441.1:n.656-244del
ENST00000644381.1:n.234-244del
ENST00000307792.7:c.671-244del ENSP00000303212.3:n.671-244del
ENST00000427262.5:c.491-244del ENSP00000405052.1:n.491-244del
NM_001178129.1:c.491-244del NP_001171600.1:n.491-244del
NM_012431.2:c.671-244del NP_036563.1:n.671-244del
XM_011516715.1:c.671-244del XP_011515017.1:n.671-244del
NM_012431.3:c.671-244del MANE Select NP_036563.1:n.671-244del
NM_001178129.2:c.491-244del NP_001171600.1:n.491-244del