Canonical Allele Identifier: CA2505285651

Gene: SEMA3E

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83407513_83407514del , CM000669.2:g.83407513_83407514del	GRCh38
NC_000007.13:g.83036829_83036830del , CM000669.1:g.83036829_83036830del	GRCh37
NC_000007.12:g.82874765_82874766del	NCBI36
NG_021242.1:g.246650_246651del
NG_021242.2:g.246650_246651del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.491-275_491-274del	ENSP00000405052.1:n.491-275_491-274del
ENST00000642232.1:c.671-275_671-274del	ENSP00000494064.1:n.671-275_671-274del
ENST00000643230.2:c.671-275_671-274del MANE Select	ENSP00000496491.1:n.671-275_671-274del
ENST00000643441.1:n.656-275_656-274del
ENST00000644381.1:n.234-275_234-274del
ENST00000307792.7:c.671-275_671-274del	ENSP00000303212.3:n.671-275_671-274del
ENST00000427262.5:c.491-275_491-274del	ENSP00000405052.1:n.491-275_491-274del
NM_001178129.1:c.491-275_491-274del	NP_001171600.1:n.491-275_491-274del
NM_012431.2:c.671-275_671-274del	NP_036563.1:n.671-275_671-274del
XM_011516715.1:c.671-275_671-274del	XP_011515017.1:n.671-275_671-274del
NM_012431.3:c.671-275_671-274del MANE Select	NP_036563.1:n.671-275_671-274del
NM_001178129.2:c.491-275_491-274del	NP_001171600.1:n.491-275_491-274del