Canonical Allele Identifier: CA2683557479

Gene: SEMA3E

Linked Data

• dbSNP Id: rs2115650030
• gnomAD v4: 7-83407360-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.83407360G>T , CM000669.2:g.83407360G>T	GRCh38
NC_000007.13:g.83036676G>T , CM000669.1:g.83036676G>T	GRCh37
NC_000007.12:g.82874612G>T	NCBI36
NG_021242.1:g.246804C>A
NG_021242.2:g.246804C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427262.6:c.491-121C>A	ENSP00000405052.1:n.491-121C>A
ENST00000642232.1:c.671-121C>A	ENSP00000494064.1:n.671-121C>A
ENST00000643230.2:c.671-121C>A MANE Select	ENSP00000496491.1:n.671-121C>A
ENST00000643441.1:n.656-121C>A
ENST00000644381.1:n.234-121C>A
ENST00000307792.7:c.671-121C>A	ENSP00000303212.3:n.671-121C>A
ENST00000427262.5:c.491-121C>A	ENSP00000405052.1:n.491-121C>A
NM_001178129.1:c.491-121C>A	NP_001171600.1:n.491-121C>A
NM_012431.2:c.671-121C>A	NP_036563.1:n.671-121C>A
XM_011516715.1:c.671-121C>A	XP_011515017.1:n.671-121C>A
NM_012431.3:c.671-121C>A MANE Select	NP_036563.1:n.671-121C>A
NM_001178129.2:c.491-121C>A	NP_001171600.1:n.491-121C>A