Canonical Allele Identifier: CA1721679568
Gene: SEMA3E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83407261_83407262delinsGA , CM000669.2:g.83407261_83407262delinsGA GRCh38
NC_000007.13:g.83036577_83036578delinsGA , CM000669.1:g.83036577_83036578delinsGA GRCh37
NC_000007.12:g.82874513_82874514delinsGA NCBI36
NG_021242.1:g.246902_246903delinsTC
NG_021242.2:g.246902_246903delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.491-23_491-22delinsTC ENSP00000405052.1:n.491-23_491-22delinsTC
ENST00000642232.1:c.671-23_671-22delinsTC ENSP00000494064.1:n.671-23_671-22delinsTC
ENST00000643230.2:c.671-23_671-22delinsTC MANE Select ENSP00000496491.1:n.671-23_671-22delinsTC
ENST00000643441.1:n.656-23_656-22delinsTC
ENST00000644381.1:n.234-23_234-22delinsTC
ENST00000307792.7:c.671-23_671-22delinsTC ENSP00000303212.3:n.671-23_671-22delinsTC
ENST00000427262.5:c.491-23_491-22delinsTC ENSP00000405052.1:n.491-23_491-22delinsTC
NM_001178129.1:c.491-23_491-22delinsTC NP_001171600.1:n.491-23_491-22delinsTC
NM_012431.2:c.671-23_671-22delinsTC NP_036563.1:n.671-23_671-22delinsTC
XM_011516715.1:c.671-23_671-22delinsTC XP_011515017.1:n.671-23_671-22delinsTC
NM_012431.3:c.671-23_671-22delinsTC MANE Select NP_036563.1:n.671-23_671-22delinsTC
NM_001178129.2:c.491-23_491-22delinsTC NP_001171600.1:n.491-23_491-22delinsTC