Canonical Allele Identifier: CA161171439

Gene: SEMA3E

Linked Data

• dbSNP Id: rs770410848
• gnomAD v3: 7-83407474-TAAAA-T
• gnomAD v4: 7-83407474-TAAAA-T
• MyVariant Identifiers: chr7:g.83036791_83036794del (hg19) ; chr7:g.83407475_83407478del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83407475_83407478del , CM000669.2:g.83407475_83407478del	GRCh38
NC_000007.13:g.83036791_83036794del , CM000669.1:g.83036791_83036794del	GRCh37
NC_000007.12:g.82874727_82874730del	NCBI36
NG_021242.1:g.246686_246689del
NG_021242.2:g.246686_246689del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.491-239_491-236del	ENSP00000405052.1:n.491-239_491-236del
ENST00000642232.1:c.671-239_671-236del	ENSP00000494064.1:n.671-239_671-236del
ENST00000643230.2:c.671-239_671-236del MANE Select	ENSP00000496491.1:n.671-239_671-236del
ENST00000643441.1:n.656-239_656-236del
ENST00000644381.1:n.234-239_234-236del
ENST00000307792.7:c.671-239_671-236del	ENSP00000303212.3:n.671-239_671-236del
ENST00000427262.5:c.491-239_491-236del	ENSP00000405052.1:n.491-239_491-236del
NM_001178129.1:c.491-239_491-236del	NP_001171600.1:n.491-239_491-236del
NM_012431.2:c.671-239_671-236del	NP_036563.1:n.671-239_671-236del
XM_011516715.1:c.671-239_671-236del	XP_011515017.1:n.671-239_671-236del
NM_012431.3:c.671-239_671-236del MANE Select	NP_036563.1:n.671-239_671-236del
NM_001178129.2:c.491-239_491-236del	NP_001171600.1:n.491-239_491-236del