Canonical Allele Identifier: CA1721679663

Gene: SEMA3E

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83407474_83407478delinsTAAAA , CM000669.2:g.83407474_83407478delinsTAAAA	GRCh38
NC_000007.13:g.83036790_83036794delinsTAAAA , CM000669.1:g.83036790_83036794delinsTAAAA	GRCh37
NC_000007.12:g.82874726_82874730delinsTAAAA	NCBI36
NG_021242.1:g.246686_246690delinsTTTTA
NG_021242.2:g.246686_246690delinsTTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.491-239_491-235delinsTTTTA	ENSP00000405052.1:n.491-239_491-235delinsTTTTA
ENST00000642232.1:c.671-239_671-235delinsTTTTA	ENSP00000494064.1:n.671-239_671-235delinsTTTTA
ENST00000643230.2:c.671-239_671-235delinsTTTTA MANE Select	ENSP00000496491.1:n.671-239_671-235delinsTTTTA
ENST00000643441.1:n.656-239_656-235delinsTTTTA
ENST00000644381.1:n.234-239_234-235delinsTTTTA
ENST00000307792.7:c.671-239_671-235delinsTTTTA	ENSP00000303212.3:n.671-239_671-235delinsTTTTA
ENST00000427262.5:c.491-239_491-235delinsTTTTA	ENSP00000405052.1:n.491-239_491-235delinsTTTTA
NM_001178129.1:c.491-239_491-235delinsTTTTA	NP_001171600.1:n.491-239_491-235delinsTTTTA
NM_012431.2:c.671-239_671-235delinsTTTTA	NP_036563.1:n.671-239_671-235delinsTTTTA
XM_011516715.1:c.671-239_671-235delinsTTTTA	XP_011515017.1:n.671-239_671-235delinsTTTTA
NM_012431.3:c.671-239_671-235delinsTTTTA MANE Select	NP_036563.1:n.671-239_671-235delinsTTTTA
NM_001178129.2:c.491-239_491-235delinsTTTTA	NP_001171600.1:n.491-239_491-235delinsTTTTA