Canonical Allele Identifier: CA2568541009
Gene: SEMA3E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.83392440G>A , CM000669.2:g.83392440G>A GRCh38
NC_000007.13:g.83021756G>A , CM000669.1:g.83021756G>A GRCh37
NC_000007.12:g.82859692G>A NCBI36
NG_021242.1:g.261724C>T
NG_021242.2:g.261724C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000427262.6:c.1487+115C>T ENSP00000405052.1:n.1487+115C>T
ENST00000642232.1:c.1667+115C>T ENSP00000494064.1:n.1667+115C>T
ENST00000643230.2:c.1667+115C>T MANE Select ENSP00000496491.1:n.1667+115C>T
ENST00000643441.1:n.1652+115C>T
ENST00000307792.7:c.1667+115C>T ENSP00000303212.3:n.1667+115C>T
ENST00000427262.5:c.1487+115C>T ENSP00000405052.1:n.1487+115C>T
NM_001178129.1:c.1487+115C>T NP_001171600.1:n.1487+115C>T
NM_012431.2:c.1667+115C>T NP_036563.1:n.1667+115C>T
XM_011516715.1:c.1667+115C>T XP_011515017.1:n.1667+115C>T
NM_012431.3:c.1667+115C>T MANE Select NP_036563.1:n.1667+115C>T
NM_001178129.2:c.1487+115C>T NP_001171600.1:n.1487+115C>T