Canonical Allele Identifier: CA1721679557
Gene: SEMA3E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83407241_83407254delinsTATAGGAGCAAAAA , CM000669.2:g.83407241_83407254delinsTATAGGAGCAAAAA GRCh38
NC_000007.13:g.83036557_83036570delinsTATAGGAGCAAAAA , CM000669.1:g.83036557_83036570delinsTATAGGAGCAAAAA GRCh37
NC_000007.12:g.82874493_82874506delinsTATAGGAGCAAAAA NCBI36
NG_021242.1:g.246910_246923delinsTTTTTGCTCCTATA
NG_021242.2:g.246910_246923delinsTTTTTGCTCCTATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.491-15_491-2delinsTTTTTGCTCCTATA ENSP00000405052.1:n.491-15_491-2delinsTTTTTGCTCCTATA
ENST00000642232.1:c.671-15_671-2delinsTTTTTGCTCCTATA ENSP00000494064.1:n.671-15_671-2delinsTTTTTGCTCCTATA
ENST00000643230.2:c.671-15_671-2delinsTTTTTGCTCCTATA MANE Select ENSP00000496491.1:n.671-15_671-2delinsTTTTTGCTCCTATA
ENST00000643441.1:n.656-15_656-2delinsTTTTTGCTCCTATA
ENST00000644381.1:n.234-15_234-2delinsTTTTTGCTCCTATA
ENST00000307792.7:c.671-15_671-2delinsTTTTTGCTCCTATA ENSP00000303212.3:n.671-15_671-2delinsTTTTTGCTCCTATA
ENST00000427262.5:c.491-15_491-2delinsTTTTTGCTCCTATA ENSP00000405052.1:n.491-15_491-2delinsTTTTTGCTCCTATA
NM_001178129.1:c.491-15_491-2delinsTTTTTGCTCCTATA NP_001171600.1:n.491-15_491-2delinsTTTTTGCTCCTATA
NM_012431.2:c.671-15_671-2delinsTTTTTGCTCCTATA NP_036563.1:n.671-15_671-2delinsTTTTTGCTCCTATA
XM_011516715.1:c.671-15_671-2delinsTTTTTGCTCCTATA XP_011515017.1:n.671-15_671-2delinsTTTTTGCTCCTATA
NM_012431.3:c.671-15_671-2delinsTTTTTGCTCCTATA MANE Select NP_036563.1:n.671-15_671-2delinsTTTTTGCTCCTATA
NM_001178129.2:c.491-15_491-2delinsTTTTTGCTCCTATA NP_001171600.1:n.491-15_491-2delinsTTTTTGCTCCTATA