Canonical Allele Identifier: CA2683557445

Gene: SEMA3E

Linked Data

• gnomAD v4: 7-83407297-A-AAGTTATTCC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83407299_83407307dup , CM000669.2:g.83407299_83407307dup	GRCh38
NC_000007.13:g.83036615_83036623dup , CM000669.1:g.83036615_83036623dup	GRCh37
NC_000007.12:g.82874551_82874559dup	NCBI36
NG_021242.1:g.246858_246866dup
NG_021242.2:g.246858_246866dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.491-67_491-59dup	ENSP00000405052.1:n.491-67_491-59dup
ENST00000642232.1:c.671-67_671-59dup	ENSP00000494064.1:n.671-67_671-59dup
ENST00000643230.2:c.671-67_671-59dup MANE Select	ENSP00000496491.1:n.671-67_671-59dup
ENST00000643441.1:n.656-67_656-59dup
ENST00000644381.1:n.234-67_234-59dup
ENST00000307792.7:c.671-67_671-59dup	ENSP00000303212.3:n.671-67_671-59dup
ENST00000427262.5:c.491-67_491-59dup	ENSP00000405052.1:n.491-67_491-59dup
NM_001178129.1:c.491-67_491-59dup	NP_001171600.1:n.491-67_491-59dup
NM_012431.2:c.671-67_671-59dup	NP_036563.1:n.671-67_671-59dup
XM_011516715.1:c.671-67_671-59dup	XP_011515017.1:n.671-67_671-59dup
NM_012431.3:c.671-67_671-59dup MANE Select	NP_036563.1:n.671-67_671-59dup
NM_001178129.2:c.491-67_491-59dup	NP_001171600.1:n.491-67_491-59dup